rs_ID |
Location |
Functional Annotation |
rs1023091 |
Chr6:44975022(Fwd) |
NMD_transcript_variant; intron_variant |
rs4714830 |
Chr6:44955528(Fwd) |
NMD_transcript_variant; intron_variant |
rs13209827 |
Chr6:44998632(Fwd) |
NMD_transcript_variant; intron_variant |
rs12214778 |
Chr6:44924412(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs13205113 |
Chr6:45003990(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948197 |
Chr6:44967490(Fwd) |
NMD_transcript_variant; intron_variant |
rs12528762 |
Chr6:45004185(Fwd) |
NMD_transcript_variant; intron_variant |
rs2396372 |
Chr6:44966867(Fwd) |
NMD_transcript_variant; intron_variant |
rs13211006 |
Chr6:45023076(Fwd) |
NMD_transcript_variant; intron_variant |
rs1041332 |
Chr6:45012811(Fwd) |
NMD_transcript_variant; intron_variant |
rs7745506 |
Chr6:45030010(Fwd) |
NMD_transcript_variant; intron_variant |
rs1329710 |
Chr6:44969125(Fwd) |
NMD_transcript_variant; intron_variant |
rs12215263 |
Chr6:44831364(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799973 |
Chr6:44823727(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948176 |
Chr6:44833913(Fwd) |
NMD_transcript_variant; intron_variant |
rs4714836 |
Chr6:45019777(Fwd) |
NMD_transcript_variant; intron_variant |
rs9367210 |
Chr6:44863395(Fwd) |
NMD_transcript_variant; intron_variant |
rs6924185 |
Chr6:45017228(Fwd) |
NMD_transcript_variant; intron_variant |
rs4714828 |
Chr6:44846008(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799979 |
Chr6:44845514(Fwd) |
NMD_transcript_variant; intron_variant |
rs608941 |
Chr6:44888740(Fwd) |
NMD_transcript_variant; intron_variant |
rs10484627 |
Chr6:44884267(Fwd) |
NMD_transcript_variant; intron_variant |
rs12196818 |
Chr6:44911414(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948185 |
Chr6:44901727(Fwd) |
NMD_transcript_variant; intron_variant |
rs4512220 |
Chr6:44923138(Fwd) |
5_prime_UTR_variant; NMD_transcript_variant; intron_variant |
rs9472414 |
Chr6:44946506(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799974 |
Chr6:44824948(Fwd) |
NMD_transcript_variant; intron_variant |
rs6919161 |
Chr6:44888117(Fwd) |
NMD_transcript_variant; intron_variant |
rs16869119 |
Chr6:44814892(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799972 |
Chr6:44823273(Fwd) |
NMD_transcript_variant; intron_variant |
rs7769218 |
Chr6:44783457(Fwd) |
NMD_transcript_variant; intron_variant |
rs2139863 |
Chr6:44796139(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs1028944 |
Chr6:44989519(Fwd) |
NMD_transcript_variant; intron_variant |
rs13201942 |
Chr6:45003827(Fwd) |
NMD_transcript_variant; intron_variant |
rs4714834 |
Chr6:44978416(Fwd) |
NMD_transcript_variant; intron_variant |
rs12528232 |
Chr6:44982593(Fwd) |
NMD_transcript_variant; synonymous_variant |
rs35687006 |
Chr6:44956622(Fwd) |
NMD_transcript_variant; intron_variant |
rs1159131 |
Chr6:44972209(Fwd) |
NMD_transcript_variant; intron_variant |
rs9296450 |
Chr6:44953786(Fwd) |
NMD_transcript_variant; intron_variant |
rs1360195 |
Chr6:44931331(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799987 |
Chr6:44925834(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs1329715 |
Chr6:44909515(Fwd) |
NMD_transcript_variant; intron_variant |
rs12530016 |
Chr6:44866322(Fwd) |
NMD_transcript_variant; intron_variant |
rs12529522 |
Chr6:44865520(Fwd) |
NMD_transcript_variant; intron_variant |
rs13206526 |
Chr6:44816181(Fwd) |
NMD_transcript_variant; intron_variant |
rs3823252 |
Chr6:44810418(Fwd) |
NMD_transcript_variant; intron_variant |
rs9472376 |
Chr6:44800247(Fwd) |
NMD_transcript_variant; intron_variant |
rs542444 |
Chr6:44800015(Fwd) |
NMD_transcript_variant; intron_variant |
rs1402599 |
Chr6:44799657(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799965 |
Chr6:44798617(Fwd) |
NMD_transcript_variant; intron_variant |
rs524492 |
Chr6:44796596(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs4398713 |
Chr6:45003928(Fwd) |
NMD_transcript_variant; intron_variant |
rs1329713 |
Chr6:45004028(Fwd) |
NMD_transcript_variant; intron_variant |
rs1023090 |
Chr6:45012381(Fwd) |
NMD_transcript_variant; intron_variant |
rs9367214 |
Chr6:45025912(Fwd) |
NMD_transcript_variant; intron_variant |
rs1329716 |
Chr6:44953758(Fwd) |
NMD_transcript_variant; intron_variant |
rs7775717 |
Chr6:44967761(Fwd) |
NMD_transcript_variant; intron_variant |
rs4711809 |
Chr6:44980341(Fwd) |
NMD_transcript_variant; intron_variant |
rs7742360 |
Chr6:44998692(Fwd) |
NMD_transcript_variant; intron_variant |
rs6925017 |
Chr6:44950828(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948194 |
Chr6:44951990(Fwd) |
NMD_transcript_variant; intron_variant |
rs9357464 |
Chr6:44952441(Fwd) |
NMD_transcript_variant; intron_variant |
rs976699 |
Chr6:44952852(Fwd) |
NMD_transcript_variant; intron_variant |
rs2396369 |
Chr6:44946463(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948190 |
Chr6:44942300(Fwd) |
NMD_transcript_variant; intron_variant |
rs1360197 |
Chr6:44949630(Fwd) |
NMD_transcript_variant; intron_variant |
rs2396371 |
Chr6:44946550(Fwd) |
NMD_transcript_variant; intron_variant |
rs1521355 |
Chr6:44932755(Fwd) |
NMD_transcript_variant; intron_variant |
rs1980265 |
Chr6:44928868(Fwd) |
NMD_transcript_variant; intron_variant |
rs494982 |
Chr6:44937255(Fwd) |
NMD_transcript_variant; intron_variant |
rs636845 |
Chr6:44935341(Fwd) |
NMD_transcript_variant; intron_variant |
rs9472407 |
Chr6:44908800(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948186 |
Chr6:44903248(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948187 |
Chr6:44921320(Fwd) |
NMD_transcript_variant; intron_variant |
rs12190513 |
Chr6:44920679(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799984 |
Chr6:44893640(Fwd) |
NMD_transcript_variant; intron_variant |
rs9367211 |
Chr6:44885305(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799986 |
Chr6:44900253(Fwd) |
NMD_transcript_variant; intron_variant |
rs3778507 |
Chr6:44896803(Fwd) |
NMD_transcript_variant; intron_variant |
rs9395051 |
Chr6:44825715(Fwd) |
NMD_transcript_variant; intron_variant |
rs9369516 |
Chr6:44833598(Fwd) |
NMD_transcript_variant; intron_variant |
rs6910294 |
Chr6:44812565(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799971 |
Chr6:44819319(Fwd) |
NMD_transcript_variant; intron_variant |
rs6458415 |
Chr6:44881592(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799981 |
Chr6:44882380(Fwd) |
NMD_transcript_variant; intron_variant |
rs7754378 |
Chr6:44863106(Fwd) |
NMD_transcript_variant; intron_variant |
rs538801 |
Chr6:44875762(Fwd) |
NMD_transcript_variant; intron_variant |
rs7754698 |
Chr6:44782717(Fwd) |
NMD_transcript_variant; intron_variant |
rs6904015 |
Chr6:44785502(Fwd) |
NMD_transcript_variant; intron_variant |
rs6910749 |
Chr6:44773892(Fwd) |
downstream_gene_variant |
rs3799967 |
Chr6:44798701(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799968 |
Chr6:44805377(Fwd) |
NMD_transcript_variant; intron_variant |
rs9395049 |
Chr6:44792718(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs9369514 |
Chr6:44797271(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs4412189 |
Chr6:45023226(Fwd) |
NMD_transcript_variant; intron_variant |
rs2186062 |
Chr6:45023732(Fwd) |
NMD_transcript_variant; intron_variant |
rs12208023 |
Chr6:45024687(Fwd) |
NMD_transcript_variant; intron_variant |
rs7763450 |
Chr6:45029896(Fwd) |
NMD_transcript_variant; intron_variant |
rs1971482 |
Chr6:44991113(Fwd) |
NMD_transcript_variant; intron_variant |
rs6925467 |
Chr6:44998038(Fwd) |
NMD_transcript_variant; intron_variant |
rs1329714 |
Chr6:45003335(Fwd) |
NMD_transcript_variant; intron_variant |
rs9369529 |
Chr6:45004533(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948198 |
Chr6:45009164(Fwd) |
NMD_transcript_variant; intron_variant |
rs12529490 |
Chr6:45018251(Fwd) |
NMD_transcript_variant; intron_variant |
rs12205071 |
Chr6:45021215(Fwd) |
NMD_transcript_variant; intron_variant |
rs969211 |
Chr6:45022378(Fwd) |
NMD_transcript_variant; intron_variant |
rs9472409 |
Chr6:44926431(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs10948188 |
Chr6:44926212(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs13216116 |
Chr6:44936681(Fwd) |
NMD_transcript_variant; intron_variant |
rs13215618 |
Chr6:44936568(Fwd) |
NMD_transcript_variant; intron_variant |
rs9472416 |
Chr6:44950963(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948192 |
Chr6:44947321(Fwd) |
NMD_transcript_variant; intron_variant |
rs17424547 |
Chr6:44988970(Fwd) |
NMD_transcript_variant; intron_variant |
rs11967188 |
Chr6:44956925(Fwd) |
NMD_transcript_variant; intron_variant |
rs12525009 |
Chr6:44875843(Fwd) |
NMD_transcript_variant; intron_variant |
rs3799976 |
Chr6:44835622(Fwd) |
NMD_transcript_variant; intron_variant |
rs10948183 |
Chr6:44880881(Fwd) |
NMD_transcript_variant; intron_variant |
rs7763421 |
Chr6:44877313(Fwd) |
NMD_transcript_variant; intron_variant |
rs17422760 |
Chr6:44885288(Fwd) |
NMD_transcript_variant; intron_variant |
rs12526711 |
Chr6:44883873(Fwd) |
NMD_transcript_variant; intron_variant |
rs7749865 |
Chr6:44918406(Fwd) |
NMD_transcript_variant; intron_variant |
rs4711807 |
Chr6:44911652(Fwd) |
NMD_transcript_variant; intron_variant |