rs_ID |
Location |
Functional Annotation |
rs1488830 |
Chr11:27636885(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11030084 |
Chr11:27643725(Fwd) |
intron_variant; nc_transcript_variant |
rs879048 |
Chr11:27638934(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4074134 |
Chr11:27647285(Fwd) |
intron_variant; nc_transcript_variant |
rs6416056 |
Chr11:27646745(Fwd) |
intron_variant; nc_transcript_variant |
rs4923460 |
Chr11:27656789(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs4923457 |
Chr11:27648580(Fwd) |
intron_variant; nc_transcript_variant |
rs12419948 |
Chr11:27666984(Fwd) |
intron_variant; nc_transcript_variant |
rs4923461 |
Chr11:27656910(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10501087 |
Chr11:27670108(Fwd) |
intron_variant; nc_transcript_variant |
rs925947 |
Chr11:27667367(Fwd) |
intron_variant; nc_transcript_variant |
rs12223664 |
Chr11:27627850(Fwd) |
intron_variant; nc_transcript_variant |
rs6484320 |
Chr11:27703188(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10767651 |
Chr11:27628607(Fwd) |
intron_variant; nc_transcript_variant |
rs16917237 |
Chr11:27702383(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11030073 |
Chr11:27625942(Fwd) |
intron_variant; nc_transcript_variant |
rs11030074 |
Chr11:27626267(Fwd) |
intron_variant; nc_transcript_variant |
rs10767652 |
Chr11:27628826(Fwd) |
intron_variant; nc_transcript_variant |
rs1038660 |
Chr11:27549392(Fwd) |
intron_variant; nc_transcript_variant |
rs11030064 |
Chr11:27618016(Fwd) |
intron_variant; nc_transcript_variant |
rs6484314 |
Chr11:27550199(Fwd) |
intron_variant; nc_transcript_variant |
rs1519480 |
Chr11:27675712(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs4923451 |
Chr11:27545230(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10835210 |
Chr11:27695910(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs7127239 |
Chr11:27547379(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs6484312 |
Chr11:27541623(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7481311 |
Chr11:27583129(Fwd) |
intron_variant; nc_transcript_variant |
rs988712 |
Chr11:27563382(Fwd) |
intron_variant; nc_transcript_variant |
rs12577586 |
Chr11:27600435(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs901925 |
Chr11:27542469(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7107410 |
Chr11:27551388(Fwd) |
intron_variant; nc_transcript_variant |
rs6484313 |
Chr11:27541800(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10767647 |
Chr11:27567392(Fwd) |
intron_variant; nc_transcript_variant |
rs1519479 |
Chr11:27667531(Fwd) |
intron_variant; nc_transcript_variant |
rs10767646 |
Chr11:27559744(Fwd) |
intron_variant; nc_transcript_variant |
rs11030094 |
Chr11:27659775(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10835193 |
Chr11:27572337(Fwd) |
intron_variant; nc_transcript_variant |
rs6484311 |
Chr11:27531764(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2203877 |
Chr11:27670910(Fwd) |
intron_variant; nc_transcript_variant |
rs7125904 |
Chr11:27543003(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10835196 |
Chr11:27601335(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs11030048 |
Chr11:27582949(Fwd) |
intron_variant; nc_transcript_variant |
rs10742178 |
Chr11:27613718(Fwd) |
intron_variant; nc_transcript_variant |
rs10767649 |
Chr11:27613818(Fwd) |
intron_variant; nc_transcript_variant |
rs10734394 |
Chr11:27628412(Fwd) |
intron_variant; nc_transcript_variant |
rs7103873 |
Chr11:27700317(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7116850 |
Chr11:27645530(Fwd) |
intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs10767660 |
Chr11:27694962(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs1038659 |
Chr11:27549330(Fwd) |
intron_variant; nc_transcript_variant |
rs10835214 |
Chr11:27707168(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant |
rs10835190 |
Chr11:27544647(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2353512 |
Chr11:27679662(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant; synonymous_variant |
rs1488829 |
Chr11:27551979(Fwd) |
intron_variant; nc_transcript_variant |
rs1304100 |
Chr11:27571603(Fwd) |
intron_variant; nc_transcript_variant |
rs1906654 |
Chr11:27574408(Fwd) |
intron_variant; nc_transcript_variant |
rs10835195 |
Chr11:27577231(Fwd) |
intron_variant; nc_transcript_variant |
rs1013442 |
Chr11:27578946(Fwd) |
intron_variant; nc_transcript_variant |
rs7124596 |
Chr11:27594558(Fwd) |
intron_variant; nc_transcript_variant |
rs1114029 |
Chr11:27595981(Fwd) |
intron_variant; nc_transcript_variant |
rs4922788 |
Chr11:27611029(Fwd) |
intron_variant; nc_transcript_variant |
rs1304101 |
Chr11:27571594(Fwd) |
intron_variant; nc_transcript_variant |
rs11030075 |
Chr11:27627296(Fwd) |
intron_variant; nc_transcript_variant |
rs2101467 |
Chr11:27544359(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs10835201 |
Chr11:27618265(Fwd) |
intron_variant; nc_transcript_variant |
rs10835197 |
Chr11:27607543(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs11030067 |
Chr11:27620932(Fwd) |
intron_variant; nc_transcript_variant |
rs12361806 |
Chr11:27619569(Fwd) |
intron_variant; nc_transcript_variant |
rs7124442 |
Chr11:27677041(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs7127507 |
Chr11:27714884(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs10835189 |
Chr11:27541995(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7937150 |
Chr11:27620360(Fwd) |
intron_variant; nc_transcript_variant |
rs7937485 |
Chr11:27620473(Fwd) |
intron_variant; nc_transcript_variant |
rs12798439 |
Chr11:27621960(Fwd) |
intron_variant; nc_transcript_variant |
rs7949590 |
Chr11:27623611(Fwd) |
intron_variant; nc_transcript_variant |