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
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs2165241 0.716 0.360 15 73929861 intron variant T/C snv 0.60 15
rs3825942 0.716 0.320 15 73927241 missense variant G/A;C;T snv 0.18; 4.5E-06 15
rs11024102 0.851 0.040 11 16987058 intron variant T/C snv 0.20 7
rs3753841 0.827 0.080 1 102914362 missense variant G/A snv 0.61 0.49 7
rs4656461 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 7
rs1015213 0.851 0.040 8 51974981 intron variant C/T snv 0.14 6
rs3788317 0.851 0.040 22 19902302 intron variant G/T snv 0.30 4