rs_ID |
Location |
Functional Annotation |
rs4830569 |
ChrX:6963699(Fwd) |
downstream_gene_variant |
rs1474467 |
ChrX:6965884(Fwd) |
downstream_gene_variant |
rs868756 |
ChrX:6975782(Fwd) |
downstream_gene_variant; intron_variant; missense_variant |
rs6530046 |
ChrX:6978441(Fwd) |
intron_variant |
rs883252 |
ChrX:6970836(Fwd) |
downstream_gene_variant; intron_variant |
rs941170 |
ChrX:6972622(Fwd) |
downstream_gene_variant; intron_variant |
rs4830591 |
ChrX:7000921(Fwd) |
downstream_gene_variant; intron_variant |
rs5978250 |
ChrX:7002209(Fwd) |
downstream_gene_variant; intron_variant |
rs7889414 |
ChrX:6982765(Fwd) |
intron_variant |
rs7055130 |
ChrX:6998201(Fwd) |
downstream_gene_variant; intron_variant |
rs1131197 |
ChrX:7023678(Fwd) |
intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant |
rs4830402 |
ChrX:7030532(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4830603 |
ChrX:7010873(Fwd) |
intron_variant; nc_transcript_variant |
rs1465066 |
ChrX:7008197(Fwd) |
intron_variant; nc_transcript_variant |
rs1534275 |
ChrX:7007600(Fwd) |
intron_variant; nc_transcript_variant |
rs5934477 |
ChrX:7014767(Fwd) |
intron_variant; nc_transcript_variant |
rs7050772 |
ChrX:7041556(Fwd) |
intron_variant; nc_transcript_variant |
rs5978210 |
ChrX:6962892(Fwd) |
downstream_gene_variant |
rs4830607 |
ChrX:7030680(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs6530042 |
ChrX:6964978(Fwd) |
downstream_gene_variant |
rs4830570 |
ChrX:6965591(Fwd) |
downstream_gene_variant |
rs5978950 |
ChrX:7020383(Fwd) |
intron_variant; nc_transcript_variant |
rs1474468 |
ChrX:6966059(Fwd) |
downstream_gene_variant |
rs10458 |
ChrX:6968011(Fwd) |
3_prime_UTR_variant |
rs5978831 |
ChrX:6970004(Fwd) |
intron_variant |
rs5978965 |
ChrX:7024974(Fwd) |
intron_variant; nc_transcript_variant |
rs5978836 |
ChrX:6974672(Fwd) |
downstream_gene_variant; intron_variant |
rs2890114 |
ChrX:7021602(Fwd) |
intron_variant; nc_transcript_variant |
rs6530047 |
ChrX:6978648(Fwd) |
intron_variant |
rs7891838 |
ChrX:6979109(Fwd) |
intron_variant |
rs5978283 |
ChrX:7041732(Fwd) |
intron_variant; nc_transcript_variant |
rs6530048 |
ChrX:6979859(Fwd) |
intron_variant |
rs3747390 |
ChrX:6995537(Fwd) |
intron_variant |
rs11095350 |
ChrX:6984092(Fwd) |
intron_variant |
rs1997185 |
ChrX:6996913(Fwd) |
intron_variant |
rs4830578 |
ChrX:6980322(Fwd) |
intron_variant |
rs4830396 |
ChrX:6992750(Fwd) |
intron_variant |
rs4504832 |
ChrX:6986549(Fwd) |
intron_variant |
rs7051403 |
ChrX:6994640(Fwd) |
intron_variant |
rs4830580 |
ChrX:6985694(Fwd) |
intron_variant |
rs4830579 |
ChrX:6983461(Fwd) |
intron_variant |
rs4240139 |
ChrX:6991678(Fwd) |
intron_variant |
rs7056478 |
ChrX:6986388(Fwd) |
intron_variant |
rs6530049 |
ChrX:6988778(Fwd) |
intron_variant |
rs6530045 |
ChrX:6978326(Fwd) |
intron_variant |
rs1997184 |
ChrX:6996732(Fwd) |
intron_variant |
rs5978851 |
ChrX:6982968(Fwd) |
intron_variant |
rs2379206 |
ChrX:6995315(Fwd) |
synonymous_variant |
rs7057654 |
ChrX:7002837(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs5978220 |
ChrX:6975752(Fwd) |
downstream_gene_variant; intron_variant; missense_variant |
rs7052687 |
ChrX:7001592(Fwd) |
downstream_gene_variant; intron_variant |
rs7892096 |
ChrX:7009936(Fwd) |
intron_variant; nc_transcript_variant |
rs5978904 |
ChrX:7003707(Fwd) |
intron_variant; nc_transcript_variant |
rs878561 |
ChrX:7028304(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs12557556 |
ChrX:7014985(Fwd) |
intron_variant; nc_transcript_variant |
rs4830608 |
ChrX:7031065(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs4500243 |
ChrX:7028564(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs6530052 |
ChrX:7033094(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1880880 |
ChrX:7034601(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs5978279 |
ChrX:7037185(Fwd) |
intron_variant; nc_transcript_variant |
rs4830613 |
ChrX:7041090(Fwd) |
intron_variant; nc_transcript_variant |
rs6530053 |
ChrX:7041357(Fwd) |
intron_variant; nc_transcript_variant |
rs12388823 |
ChrX:7044081(Fwd) |
intron_variant; nc_transcript_variant |
rs5978295 |
ChrX:7056721(Fwd) |
intron_variant; nc_transcript_variant |
rs5979036 |
ChrX:7059036(Fwd) |
intron_variant; nc_transcript_variant |
rs6530056 |
ChrX:7061642(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2379207 |
ChrX:6995417(Fwd) |
synonymous_variant |
rs869505 |
ChrX:7047942(Fwd) |
intron_variant; nc_transcript_variant |
rs7887251 |
ChrX:7052902(Fwd) |
intron_variant; nc_transcript_variant |
rs1967431 |
ChrX:7064178(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs941171 |
ChrX:7066723(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs12689752 |
ChrX:6988198(Fwd) |
intron_variant |
rs6530058 |
ChrX:7068997(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs12557020 |
ChrX:6984240(Fwd) |
intron_variant |
rs5979051 |
ChrX:7069529(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs12556704 |
ChrX:6995732(Fwd) |
intron_variant |
rs12558888 |
ChrX:6995693(Fwd) |
intron_variant |
rs17326009 |
ChrX:7002158(Fwd) |
downstream_gene_variant; intron_variant |
rs4830590 |
ChrX:7000468(Fwd) |
downstream_gene_variant; intron_variant |
rs4830399 |
ChrX:7005180(Fwd) |
intron_variant; nc_transcript_variant |
rs1465067 |
ChrX:7007959(Fwd) |
intron_variant; nc_transcript_variant |
rs1125438 |
ChrX:7057677(Fwd) |
intron_variant; nc_transcript_variant |
rs941172 |
ChrX:7066604(Fwd) |
downstream_gene_variant; upstream_gene_variant |
rs4830571 |
ChrX:6965693(Fwd) |
downstream_gene_variant |
rs2379204 |
ChrX:6973298(Fwd) |
downstream_gene_variant; intron_variant |