Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1373756 1.000 0.120 18 52259936 intergenic variant C/T snv 0.24 2
rs221236 1.000 0.120 7 157529938 downstream gene variant G/A snv 0.96 2
rs1473418
BCL2
1.000 0.080 18 63319316 5 prime UTR variant C/G snv 0.98 2
rs1950252
BCL2L2-PABPN1 ; BCL2L2
1.000 0.080 14 23309489 3 prime UTR variant A/G snv 0.93 2
rs1045487
CASP8
1.000 0.080 2 201284973 synonymous variant G/A snv 9.5E-02 0.10 2
rs34329
CDKN1B
1.000 0.080 12 12720299 intron variant G/C snv 0.61 2
rs16914640
CLEC2D
1.000 0.120 12 9669791 missense variant C/G;T snv 0.14; 4.0E-06 2
rs2292566
EPHX1
1.000 0.080 1 225831952 synonymous variant G/A snv 2
rs11130760
FHIT
1.000 0.080 3 60210809 intron variant G/T snv 0.12 2
rs771266873
GORASP1
1.000 0.080 3 39098828 missense variant G/A;C snv 2
rs221636
LIN28B
1.000 0.120 6 105082089 3 prime UTR variant T/A snv 0.82 2
rs1271546630
MPO
1.000 0.120 17 58277848 missense variant G/A;C snv 2
rs3092904
RB1
1.000 0.080 13 48477345 intron variant T/A snv 0.24 0.20 2
rs17071138
SERPINB5
1.000 0.080 18 63476675 upstream gene variant T/C snv 2.9E-02 2
rs8089104
SERPINB5
1.000 0.080 18 63480916 intron variant C/T snv 0.50 2
rs3757769
SND1
1.000 0.080 7 127901009 intron variant A/G snv 9.7E-02 2
rs7778413
SND1
1.000 0.080 7 127717662 intron variant T/C snv 0.23 2
rs7085532
TCF7L2
1.000 0.080 10 113099704 intron variant G/A snv 0.72 2
rs587778718
TP53
1.000 0.080 17 7674959 missense variant G/A;C;T snv 4.0E-06; 1.2E-05; 4.0E-06 2
rs563691424
WNK1
1.000 0.080 12 753860 missense variant C/T snv 6.2E-05 2.1E-05 2
rs2040639
XRCC2
1.000 0.080 7 152678103 upstream gene variant T/C;G snv 2
rs33438
ZNF536
1.000 0.080 19 30454165 intron variant G/A snv 0.50 2
rs7834169 0.925 0.120 8 27052774 upstream gene variant C/G snv 0.16 3
rs511044
CASP5
0.925 0.120 11 105024783 upstream gene variant T/C snv 3
rs9849237
CNTN4
1.000 0.080 3 2633505 intron variant C/T snv 0.25 3