Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17381664
ZZZ3
1.000 0.080 1 77582646 intron variant T/C snv 0.29 3
rs774006043
ZPR1 ; APOA5
0.925 0.080 11 116790561 missense variant C/T snv 3
rs2047937
ZNF423
0.925 0.120 16 49830880 intron variant C/T snv 0.50 5
rs9825174
XXYLT1
0.925 0.120 3 195118855 intron variant C/A;G;T snv 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1799782
XRCC1
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs9923451
WWOX
1.000 0.080 16 78918542 intron variant A/C;G snv 1
rs35034312
WNT10B
1.000 0.080 12 48966364 missense variant G/A snv 1.1E-02 1.2E-02 1
rs553395822
WNT10B
1.000 0.080 12 48967974 missense variant C/T snv 1.9E-04 7.0E-05 1
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs3809508
WDR73 ; NMB
1.000 0.080 15 84655660 intron variant T/C snv 0.86 1
rs2441666
WASHC1
1.000 0.080 9 63957 intron variant C/A snv 1
rs1802295
VPS26A
0.882 0.200 10 69171718 3 prime UTR variant C/T snv 0.22 4
rs35400704
VGF
1.000 0.080 7 101163271 stop gained C/A;G;T snv 6.4E-06 1
rs752907384
VEGFA
0.827 0.200 6 43782077 missense variant C/G;T snv 8.0E-06 6
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2239179
VDR
0.790 0.200 12 47863983 intron variant T/C snv 0.39 9
rs2239185
VDR
0.807 0.320 12 47850776 intron variant G/A snv 0.54 6
rs3847987
VDR
0.882 0.160 12 47844285 3 prime UTR variant C/A snv 0.12 4
rs3782905
VDR
0.882 0.200 12 47872384 intron variant G/C snv 0.29 3
rs12721377
VDR
1.000 0.080 12 47901568 intron variant T/C snv 2.2E-02 1
rs602990
VAV2
1.000 0.080 9 133778872 missense variant T/A;C snv 4.0E-06; 0.49 1
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 11
rs150016118
UCP3
0.882 0.120 11 74006339 missense variant A/G snv 1.7E-05 6.3E-05 6