Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs6982751
XKR6
0.925 0.120 8 10955964 intron variant C/G;T snv 2
rs2416257
WDR36
0.882 0.160 5 111099792 intron variant C/G;T snv 5
rs1043828
WDR36
1.000 0.080 5 111128310 3 prime UTR variant T/C;G snv 2
rs6736411
WDPCP
0.925 0.120 2 63446926 intron variant G/A snv 0.78 2
rs148728975
VPS13D
1.000 0.080 1 12359827 intron variant G/A snv 3.7E-03 1
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs833069
VEGFA
0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv 5
rs3025020
VEGFA
0.882 0.240 6 43781373 non coding transcript exon variant C/T snv 0.24 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
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
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2239185
VDR
0.807 0.320 12 47850776 intron variant G/A snv 0.54 6
rs3782905
VDR
0.882 0.200 12 47872384 intron variant G/C snv 0.29 3
rs7521681
VAV3
0.925 0.120 1 107779913 intron variant G/A snv 0.15 2
rs7169793
UNC13C
1.000 0.080 15 53872840 intergenic variant G/C snv 0.93 1
rs7864027
UHRF2
1.000 0.080 9 6504189 intron variant A/C;T snv 1
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs272474
UBE2QL1
1.000 0.080 5 6462225 intron variant A/G snv 0.93 1
rs1887704
UBAC2
0.925 0.080 13 99322238 intron variant C/G snv 0.55 2
rs59186511
UBAC2
1.000 0.080 13 99333984 intron variant C/T snv 0.13 1
rs766793834
TSPAN31
0.925 0.080 12 57747080 missense variant C/G;T snv 4.0E-06; 8.0E-06 2