rs_ID |
Location |
Functional Annotation |
rs12585267 |
Chr13:42759971(Fwd) |
intron_variant; nc_transcript_variant |
rs4598803 |
Chr13:42762871(Fwd) |
intron_variant; nc_transcript_variant |
rs2122247 |
Chr13:42763140(Fwd) |
intron_variant; nc_transcript_variant |
rs12584544 |
Chr13:42768720(Fwd) |
intron_variant; nc_transcript_variant |
rs10492441 |
Chr13:42762085(Fwd) |
intron_variant; nc_transcript_variant |
rs10492439 |
Chr13:42762316(Fwd) |
intron_variant; nc_transcript_variant |
rs12870816 |
Chr13:42767252(Fwd) |
intron_variant; nc_transcript_variant |
rs12870823 |
Chr13:42767261(Fwd) |
intron_variant; nc_transcript_variant |
rs1012053 |
Chr13:42653437(Fwd) |
intron_variant |
rs2253650 |
Chr13:42656841(Fwd) |
intron_variant |
rs12583267 |
Chr13:42775439(Fwd) |
intron_variant; nc_transcript_variant |
rs1184924 |
Chr13:42704400(Fwd) |
intron_variant |
rs1170109 |
Chr13:42779694(Fwd) |
intron_variant; nc_transcript_variant |
rs585206 |
Chr13:42689853(Fwd) |
intron_variant |
rs9315891 |
Chr13:42699079(Fwd) |
intron_variant |
rs9533003 |
Chr13:42699604(Fwd) |
intron_variant |
rs912875 |
Chr13:42677238(Fwd) |
intron_variant |
rs7981733 |
Chr13:42690060(Fwd) |
intron_variant |
rs1170171 |
Chr13:42689717(Fwd) |
intron_variant |
rs1170155 |
Chr13:42702711(Fwd) |
intron_variant |
rs2767389 |
Chr13:42681678(Fwd) |
intron_variant |
rs686810 |
Chr13:42686172(Fwd) |
intron_variant |
rs9594693 |
Chr13:42744103(Fwd) |
downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1170158 |
Chr13:42701941(Fwd) |
intron_variant |
rs13378817 |
Chr13:42740933(Fwd) |
intron_variant; nc_transcript_variant |
rs670676 |
Chr13:42701739(Fwd) |
intron_variant |
rs2038883 |
Chr13:42705815(Fwd) |
intron_variant |
rs1177637 |
Chr13:42692823(Fwd) |
intron_variant |
rs3742261 |
Chr13:42703682(Fwd) |
intron_variant; splice_region_variant |
rs1170173 |
Chr13:42688615(Fwd) |
intron_variant |
rs9533005 |
Chr13:42706147(Fwd) |
intron_variant |
rs1667559 |
Chr13:42798106(Fwd) |
intron_variant; nc_transcript_variant |
rs685951 |
Chr13:42686359(Fwd) |
intron_variant |
rs2038882 |
Chr13:42705435(Fwd) |
intron_variant |
rs1170187 |
Chr13:42679835(Fwd) |
intron_variant |
rs10467371 |
Chr13:42740328(Fwd) |
intron_variant; nc_transcript_variant |
rs1170188 |
Chr13:42678971(Fwd) |
intron_variant |
rs17520002 |
Chr13:42739775(Fwd) |
intron_variant; nc_transcript_variant |
rs9285148 |
Chr13:42704669(Fwd) |
intron_variant |
rs1170190 |
Chr13:42675667(Fwd) |
intron_variant |
rs12865430 |
Chr13:42736013(Fwd) |
intron_variant; nc_transcript_variant |
rs9533007 |
Chr13:42710235(Fwd) |
intron_variant; upstream_gene_variant |
rs17645393 |
Chr13:42734840(Fwd) |
intron_variant; nc_transcript_variant |
rs9590671 |
Chr13:42726974(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs12876965 |
Chr13:42712741(Fwd) |
intron_variant; upstream_gene_variant |
rs12585075 |
Chr13:42711224(Fwd) |
intron_variant; upstream_gene_variant |
rs1886811 |
Chr13:42722064(Fwd) |
intron_variant; nc_transcript_variant |
rs682573 |
Chr13:42708655(Fwd) |
intron_variant; upstream_gene_variant |
rs965256 |
Chr13:42719209(Fwd) |
intron_variant; nc_transcript_variant |
rs1170178 |
Chr13:42705808(Fwd) |
intron_variant |
rs619659 |
Chr13:42706673(Fwd) |
intron_variant |
rs1750017 |
Chr13:42704451(Fwd) |
intron_variant |
rs4624054 |
Chr13:42723462(Fwd) |
intron_variant; nc_transcript_variant |
rs7984523 |
Chr13:42678357(Fwd) |
intron_variant |
rs12856887 |
Chr13:42686601(Fwd) |
intron_variant |
rs9645982 |
Chr13:42681425(Fwd) |
intron_variant |
rs9315887 |
Chr13:42671625(Fwd) |
intron_variant |
rs1115398 |
Chr13:42669119(Fwd) |
intron_variant |
rs7986454 |
Chr13:42703394(Fwd) |
intron_variant |
rs627089 |
Chr13:42698918(Fwd) |
intron_variant |
rs9594677 |
Chr13:42694222(Fwd) |
intron_variant |
rs9645983 |
Chr13:42687303(Fwd) |
intron_variant |
rs9525573 |
Chr13:42677500(Fwd) |
intron_variant |
rs9525570 |
Chr13:42675006(Fwd) |
intron_variant |
rs9525569 |
Chr13:42674830(Fwd) |
intron_variant |
rs9532998 |
Chr13:42673336(Fwd) |
intron_variant |
rs9532993 |
Chr13:42664617(Fwd) |
intron_variant |
rs9315897 |
Chr13:42738982(Fwd) |
intron_variant; nc_transcript_variant |
rs10492444 |
Chr13:42734389(Fwd) |
intron_variant; nc_transcript_variant |
rs9590664 |
Chr13:42695704(Fwd) |
intron_variant |
rs716934 |
Chr13:42719995(Fwd) |
intron_variant; nc_transcript_variant |
rs9532997 |
Chr13:42673177(Fwd) |
intron_variant |
rs9590666 |
Chr13:42712871(Fwd) |
intron_variant; upstream_gene_variant |
rs9525576 |
Chr13:42685989(Fwd) |
intron_variant |
rs9533002 |
Chr13:42689009(Fwd) |
intron_variant |
rs9562380 |
Chr13:42704847(Fwd) |
intron_variant |
rs7983995 |
Chr13:42708231(Fwd) |
intron_variant; upstream_gene_variant |
rs7327259 |
Chr13:42709345(Fwd) |
intron_variant; upstream_gene_variant |
rs7329683 |
Chr13:42721707(Fwd) |
intron_variant; nc_transcript_variant |
rs9566931 |
Chr13:42724498(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs9533015 |
Chr13:42726118(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs9533019 |
Chr13:42730949(Fwd) |
intron_variant; nc_transcript_variant |
rs10459372 |
Chr13:42732565(Fwd) |
intron_variant; nc_transcript_variant |
rs9533020 |
Chr13:42733029(Fwd) |
intron_variant; nc_transcript_variant |
rs9315894 |
Chr13:42733977(Fwd) |
intron_variant; nc_transcript_variant |
rs1555819 |
Chr13:42741873(Fwd) |
intron_variant; nc_transcript_variant |