Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs17216707 20 54115823 intergenic variant T/C snv 0.17 6
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 5
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 5
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5
rs6127099 20 54114863 intergenic variant A/T snv 0.28 5
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 4
rs13191445 0.925 0.120 6 26015261 upstream gene variant G/A snv 5.6E-02 4
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 4
rs7123489 1.000 0.080 11 65756781 intron variant C/A snv 0.29 4
rs10874312 1 82478888 intron variant G/A snv 0.70 3
rs10941191 1.000 0.040 5 34504693 intergenic variant C/A;T snv 3
rs12428035 13 95648618 upstream gene variant C/A;T snv 3
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 3
rs1974990 1.000 0.040 2 169790406 non coding transcript exon variant G/T snv 0.90 3
rs200950799 1.000 0.040 12 17004185 intergenic variant C/T snv 1.1E-02 3