Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10062757 5 62239297 intergenic variant T/C snv 0.35 1
rs10821556 9 134077014 upstream gene variant C/A snv 0.37 1
rs10900828 5 134500603 upstream gene variant T/A;C;G snv 1
rs11356207 17 64307290 downstream gene variant TTTT/-;T;TT;TTT;TTTTT delins 0.49 1
rs11653144 17 29348208 upstream gene variant C/T snv 0.43 1
rs118033845 10 11794093 TF binding site variant G/A snv 2.6E-02 1
rs11893307 2 190863318 regulatory region variant G/A snv 0.21 1
rs12645070 4 56903940 upstream gene variant G/A snv 0.19 1
rs13257813 8 19167306 intron variant G/A snv 0.70 1
rs1328599 10 95294018 upstream gene variant G/T snv 0.92 1
rs150273160 12 32665726 intergenic variant CGTGTG/- delins 1.6E-05 1
rs157198 1 28877395 upstream gene variant T/A;C snv 1
rs1684041 15 64908605 intron variant C/T snv 0.19 1
rs17655730 11 270715 intergenic variant T/C snv 0.20 1
rs185523698 20 58977406 intron variant C/T snv 1.6E-02 1
rs2113036 19 16106643 upstream gene variant T/C snv 0.28 1
rs2138852 17 29376331 intron variant C/G;T snv 1
rs236907 1 171675446 upstream gene variant G/A snv 0.15 1
rs2546976 5 160173207 intergenic variant T/C snv 0.70 1
rs2950390 12 56661507 downstream gene variant C/G;T snv 1
rs3131057 6 30794316 downstream gene variant T/C snv 0.61 1
rs35304300 6 139536204 intron variant A/G snv 0.15 1
rs35547687 7 158833186 upstream gene variant -/A;AA delins 1
rs4812048 20 59012716 intergenic variant C/T snv 0.15 1
rs528863805 16 29855475 downstream gene variant T/-;TT;TTT delins 1