Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs121908117 0.708 0.440 3 48466707 missense variant G/A snv 17
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs6568431 0.790 0.320 6 106140931 intron variant A/C snv 0.61 7