Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1390282714
MAPK1
0.925 0.080 22 21769233 missense variant C/A;T snv 4.0E-06; 4.0E-06 2
rs1425164489
TCN2
0.925 0.080 22 30617374 missense variant A/G;T snv 4.0E-06 2
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 15
rs6068816
CYP24A1
0.752 0.200 20 54164552 synonymous variant C/T snv 0.12 8.9E-02 12
rs2585428
CYP24A1
0.763 0.200 20 54170358 intron variant C/T snv 0.46 11
rs6022999
CYP24A1
0.790 0.160 20 54171474 intron variant A/G snv 0.36 9
rs4809960
CYP24A1
0.807 0.240 20 54169534 intron variant T/C snv 0.20 8
rs8124792
CYP24A1
0.827 0.120 20 54150268 downstream gene variant G/A snv 7.8E-02 6
rs121913314
SRC
0.851 0.120 20 37403359 stop gained C/T snv 5
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
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 13
rs2228612
DNMT1
0.763 0.160 19 10162696 missense variant T/A;C;G snv 0.14 12
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 11
rs1017621656
TGFB1
0.925 0.080 19 41352923 missense variant A/C;G snv 1.9E-05 3
rs2304204
BCL2L12 ; IRF3
0.882 0.160 19 49665763 5 prime UTR variant T/C snv 0.39 3
rs779066883
MIR3188 ; JUND
0.925 0.080 19 18281184 missense variant G/A snv 6.2E-06 2
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25