rs_ID |
Location |
Functional Annotation |
rs7954927 |
Chr12:79798573(Fwd) |
intron_variant; nc_transcript_variant |
rs17005561 |
Chr12:79800344(Fwd) |
intron_variant; nc_transcript_variant |
rs1465045 |
Chr12:79788631(Fwd) |
intron_variant; nc_transcript_variant |
rs11114107 |
Chr12:79799216(Fwd) |
intron_variant; nc_transcript_variant |
rs12423434 |
Chr12:79801525(Fwd) |
intron_variant; nc_transcript_variant |
rs1245774 |
Chr12:79760767(Fwd) |
intron_variant; nc_transcript_variant |
rs17294719 |
Chr12:79812271(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1405495 |
Chr12:79799306(Fwd) |
intron_variant; nc_transcript_variant |
rs11114116 |
Chr12:79831956(Fwd) |
intron_variant; nc_transcript_variant |
rs1526955 |
Chr12:79800028(Fwd) |
intron_variant; nc_transcript_variant |
rs1405497 |
Chr12:79804808(Fwd) |
intron_variant; nc_transcript_variant |
rs7295888 |
Chr12:79807346(Fwd) |
intron_variant; nc_transcript_variant |
rs4609662 |
Chr12:79802176(Fwd) |
intron_variant; nc_transcript_variant |
rs1358243 |
Chr12:79803909(Fwd) |
intron_variant; nc_transcript_variant |
rs17041667 |
Chr12:79811286(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7308297 |
Chr12:79777844(Fwd) |
intron_variant; nc_transcript_variant |
rs17005588 |
Chr12:79809256(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11612225 |
Chr12:79810422(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11114122 |
Chr12:79847040(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11114088 |
Chr12:79794919(Fwd) |
intron_variant; nc_transcript_variant |
rs2400395 |
Chr12:79778358(Fwd) |
intron_variant; nc_transcript_variant |
rs7966962 |
Chr12:79779417(Fwd) |
intron_variant; nc_transcript_variant |
rs11114112 |
Chr12:79812829(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11114027 |
Chr12:79775248(Fwd) |
intron_variant; nc_transcript_variant |
rs11113987 |
Chr12:79760464(Fwd) |
intron_variant; nc_transcript_variant |
rs11113980 |
Chr12:79759364(Fwd) |
intron_variant; nc_transcript_variant |
rs1245765 |
Chr12:79777291(Fwd) |
intron_variant; nc_transcript_variant |
rs1245767 |
Chr12:79776820(Fwd) |
intron_variant; nc_transcript_variant |
rs1245778 |
Chr12:79768171(Fwd) |
intron_variant; nc_transcript_variant |
rs12371960 |
Chr12:79778446(Fwd) |
intron_variant; nc_transcript_variant |
rs1245766 |
Chr12:79776882(Fwd) |
intron_variant; nc_transcript_variant |
rs1245770 |
Chr12:79775359(Fwd) |
intron_variant; nc_transcript_variant |
rs7135647 |
Chr12:79839153(Fwd) |
intron_variant; nc_transcript_variant |
rs7315113 |
Chr12:79832584(Fwd) |
intron_variant; nc_transcript_variant |
rs9788036 |
Chr12:79779307(Fwd) |
intron_variant; nc_transcript_variant |
rs1465051 |
Chr12:79778230(Fwd) |
intron_variant; nc_transcript_variant |
rs1465044 |
Chr12:79788930(Fwd) |
intron_variant; nc_transcript_variant |
rs10778657 |
Chr12:79784735(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10861976 |
Chr12:79794658(Fwd) |
intron_variant; nc_transcript_variant |
rs10861975 |
Chr12:79794590(Fwd) |
intron_variant; nc_transcript_variant |
rs10861941 |
Chr12:79760388(Fwd) |
intron_variant; nc_transcript_variant |
rs2895728 |
Chr12:79802302(Fwd) |
intron_variant; nc_transcript_variant |
rs1465048 |
Chr12:79798409(Fwd) |
intron_variant; nc_transcript_variant |
rs1465049 |
Chr12:79798494(Fwd) |
intron_variant; nc_transcript_variant |
rs7133421 |
Chr12:79798167(Fwd) |
intron_variant; nc_transcript_variant |
rs1465047 |
Chr12:79798317(Fwd) |
intron_variant; nc_transcript_variant |
rs1465046 |
Chr12:79797095(Fwd) |
intron_variant; nc_transcript_variant |
rs7303658 |
Chr12:79797902(Fwd) |
intron_variant; nc_transcript_variant |
rs11608780 |
Chr12:79795919(Fwd) |
intron_variant; nc_transcript_variant |
rs11608808 |
Chr12:79796144(Fwd) |
intron_variant; nc_transcript_variant |
rs10506815 |
Chr12:79793312(Fwd) |
intron_variant; nc_transcript_variant |
rs1405493 |
Chr12:79793964(Fwd) |
intron_variant; nc_transcript_variant |
rs4578461 |
Chr12:79790779(Fwd) |
intron_variant; nc_transcript_variant |
rs12581451 |
Chr12:79791607(Fwd) |
intron_variant; nc_transcript_variant |
rs17005544 |
Chr12:79785690(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs17005546 |
Chr12:79790026(Fwd) |
intron_variant; nc_transcript_variant |
rs2701566 |
Chr12:79770528(Fwd) |
intron_variant; nc_transcript_variant |
rs12579420 |
Chr12:79789319(Fwd) |
intron_variant; nc_transcript_variant |
rs7971881 |
Chr12:79781339(Fwd) |
feature_truncation; intron_variant; nc_transcript_variant |