Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 1
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 1
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 5
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3