Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs79105258 12 111280427 intron variant C/A;T snv 23
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs1057941 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs2300206 0.708 0.280 20 34002002 intron variant G/C;T snv 17
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
rs11168936 0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs2974935 0.708 0.280 1 155212052 non coding transcript exon variant G/A;C;T snv 17
rs481519 0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs115392158 0.708 0.280 6 31347004 intron variant A/G snv 17
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs12601991 0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs13114738 0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs7115242 0.851 0.120 11 117037567 intron variant A/G;T snv 16