rs_ID |
Location |
Functional Annotation |
rs11575286 |
Chr7:50612085(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs3807553 |
Chr7:50610613(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs2876830 |
Chr7:50612901(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs11575282 |
Chr7:50612707(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs1349491 |
Chr7:50614076(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs4947644 |
Chr7:50618876(Fwd) |
NMD_transcript_variant; intron_variant |
rs11765748 |
Chr7:50615616(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs10499694 |
Chr7:50614173(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs7786398 |
Chr7:50612906(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs11575334 |
Chr7:50597301(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10499696 |
Chr7:50621588(Fwd) |
NMD_transcript_variant; intron_variant |
rs11575298 |
Chr7:50610765(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs7809234 |
Chr7:50610379(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs10268819 |
Chr7:50610071(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; upstream_gene_variant |
rs2122817 |
Chr7:50567679(Fwd) |
NMD_transcript_variant; intron_variant |
rs2167364 |
Chr7:50565827(Fwd) |
NMD_transcript_variant; intron_variant |
rs11575338 |
Chr7:50596623(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11575548 |
Chr7:50530309(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs17634717 |
Chr7:50532756(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11575553 |
Chr7:50526219(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; nc_transcript_variant; non_coding_exon_variant |
rs2242041 |
Chr7:50529449(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11575404 |
Chr7:50565963(Fwd) |
NMD_transcript_variant; intron_variant |
rs1107743 |
Chr7:50569280(Fwd) |
NMD_transcript_variant; intron_variant |
rs2329367 |
Chr7:50547922(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs17634958 |
Chr7:50549880(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs11575321 |
Chr7:50605107(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11575313 |
Chr7:50606168(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17635123 |
Chr7:50575975(Fwd) |
NMD_transcript_variant; intron_variant |
rs11575322 |
Chr7:50605032(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12718572 |
Chr7:50573325(Fwd) |
NMD_transcript_variant; intron_variant |
rs13311361 |
Chr7:50549008(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs3823674 |
Chr7:50571996(Fwd) |
NMD_transcript_variant; intron_variant |
rs11980368 |
Chr7:50549939(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs4579483 |
Chr7:50546100(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12718574 |
Chr7:50573848(Fwd) |
NMD_transcript_variant; intron_variant |
rs4947577 |
Chr7:50548609(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs4329234 |
Chr7:50546006(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4433100 |
Chr7:50546037(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs3807566 |
Chr7:50564204(Fwd) |
NMD_transcript_variant; intron_variant |
rs12718529 |
Chr7:50545593(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11238138 |
Chr7:50545992(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4947535 |
Chr7:50531681(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs7785224 |
Chr7:50562361(Fwd) |
NMD_transcript_variant; intron_variant |
rs1451372 |
Chr7:50553871(Fwd) |
NMD_transcript_variant; intron_variant |
rs10899736 |
Chr7:50546925(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12718541 |
Chr7:50550144(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs2122822 |
Chr7:50552152(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs10899735 |
Chr7:50546891(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10899734 |
Chr7:50546764(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4580999 |
Chr7:50546261(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12718528 |
Chr7:50545571(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs12718527 |
Chr7:50545549(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4992502 |
Chr7:50545191(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs3887825 |
Chr7:50545093(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17634771 |
Chr7:50541554(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2876827 |
Chr7:50544975(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11771818 |
Chr7:50542175(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs2329365 |
Chr7:50544945(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs17553791 |
Chr7:50574483(Fwd) |
NMD_transcript_variant; intron_variant |
rs7803247 |
Chr7:50540743(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11575342 |
Chr7:50596357(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs730092 |
Chr7:50535754(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs11768267 |
Chr7:50533539(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs4947582 |
Chr7:50566090(Fwd) |
NMD_transcript_variant; intron_variant |
rs4948196 |
Chr7:50548651(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs11575457 |
Chr7:50547584(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs7777600 |
Chr7:50592671(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs7808025 |
Chr7:50576903(Fwd) |
NMD_transcript_variant; intron_variant |
rs2198144 |
Chr7:50574254(Fwd) |
NMD_transcript_variant; intron_variant |
rs1817074 |
Chr7:50574012(Fwd) |
NMD_transcript_variant; intron_variant |
rs7809758 |
Chr7:50573333(Fwd) |
NMD_transcript_variant; intron_variant |
rs17133877 |
Chr7:50608698(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs3779084 |
Chr7:50568735(Fwd) |
NMD_transcript_variant; intron_variant |
rs10228056 |
Chr7:50594738(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs17152020 |
Chr7:50549859(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs2329364 |
Chr7:50581699(Fwd) |
NMD_transcript_variant; intron_variant |
rs4585697 |
Chr7:50615840(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; upstream_gene_variant |
rs880028 |
Chr7:50570136(Fwd) |
NMD_transcript_variant; intron_variant |
rs12538830 |
Chr7:50591132(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs10249982 |
Chr7:50591390(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs6592963 |
Chr7:50581845(Fwd) |
NMD_transcript_variant; intron_variant |
rs12535064 |
Chr7:50591070(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs10244632 |
Chr7:50598703(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4947584 |
Chr7:50572709(Fwd) |
NMD_transcript_variant; intron_variant |
rs9918702 |
Chr7:50592082(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant |
rs3735274 |
Chr7:50596630(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2100280 |
Chr7:50580836(Fwd) |
NMD_transcript_variant; intron_variant |
rs4490786 |
Chr7:50544314(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; splice_region_variant |