Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691021 0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs111033565 0.742 0.120 7 142751938 missense variant G/A snv 1.2E-05 11
rs267606982 0.742 0.120 7 142751938 missense variant GC/AT mnv 11
rs1049074086 0.925 0.120 11 1759567 missense variant A/G snv 7.0E-06 9
rs12413624 0.851 0.120 10 118519432 intergenic variant T/A snv 0.34 5
rs2239186
VDR
0.882 0.120 12 47875627 intron variant A/C;G snv 0.17 5
rs9502893 0.827 0.120 6 1339954 intergenic variant C/G;T snv 5
rs1176026649 0.851 0.120 4 168921582 missense variant C/T snv 7.2E-06 4
rs199976573 0.925 0.120 4 88132618 missense variant C/T snv 6.4E-05 5.6E-05 4
rs2229629
HK2
0.882 0.120 2 74889400 missense variant G/A snv 6.0E-02 0.18 4
rs4759313 0.851 0.120 12 53965290 intron variant T/A snv 0.51 4
rs56053615 0.851 0.120 3 9751845 missense variant G/A;T snv 3.4E-04; 4.0E-06 4
rs78303930
NES
0.925 0.120 1 156670593 missense variant C/A;G snv 4.0E-06; 2.4E-03 4
rs7859034 0.851 0.120 9 104103411 intron variant G/T snv 0.60 4
rs786203926
ATM
0.882 0.120 11 108227678 synonymous variant T/C snv 4
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs980303898 0.851 0.120 2 162147479 missense variant T/C snv 8.0E-06 7.0E-06 4
rs11644322 0.925 0.120 16 79005703 intron variant C/T snv 0.22 3
rs1182933 1.000 0.120 12 121016819 upstream gene variant C/T snv 0.26 3
rs12029406 0.882 0.120 1 199936700 intergenic variant C/T snv 0.36 3
rs1209809979 0.925 0.120 1 45568989 missense variant A/G snv 4.0E-06 3
rs1370041903 0.925 0.120 6 161350185 stop gained G/A snv 3
rs139599857 0.882 0.120 19 43545922 missense variant C/G snv 1.6E-05 2.1E-05 3
rs150495372 0.925 0.120 4 99313834 missense variant C/T snv 3.7E-04 3