Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11456863 3 12230419 regulatory region variant T/-;TT;TTT;TTTTTTTTTTT delins 3
rs12428035 13 95648618 upstream gene variant C/A;T snv 3
rs1250229 1.000 0.040 2 215439661 upstream gene variant T/C snv 0.77 3
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 3
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 3
rs1883711 20 40551182 regulatory region variant G/C snv 2.5E-02 3
rs193084249 1 26661155 intergenic variant A/G snv 1.7E-02 3
rs2452170 19 48710247 downstream gene variant G/A;C snv 3
rs2927439 19 44739483 intergenic variant A/G snv 0.38 3
rs3902354 1 109276674 downstream gene variant C/A;T snv 3
rs4360309 8 125511281 intron variant C/G;T snv 3
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 3
rs541041 2 21072103 intergenic variant G/A snv 0.71 3
rs563290 2 21065354 intergenic variant G/A snv 0.69 3
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 3
rs661955 1 234707109 upstream gene variant G/C;T snv 3
rs74664507 1.000 0.040 9 16913838 upstream gene variant T/A snv 3
rs9297994 8 58479765 intergenic variant G/A snv 0.75 3
rs934198 2 21055901 intergenic variant G/T snv 0.26 3
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 2
rs10172650 2 20982585 intergenic variant G/A snv 0.28 2
rs10260606 7 44544952 upstream gene variant G/A;C snv 2
rs11164654 1 92502755 regulatory region variant T/C snv 0.85 2
rs113190300 19 11080015 downstream gene variant C/A;G;T snv 2
rs114067101 6 32490183 intergenic variant A/G snv 6.1E-05 2