Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4359426
CCL22
0.925 0.120 16 57358821 missense variant A/C;T snv 0.92 0.94 3
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2250889
SLC12A5-AS1 ; MMP9
0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs1997623
CAV1
0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 9
rs2740348
GEMIN4
0.851 0.160 17 746695 missense variant G/C;T snv 0.85 6
rs4245739
MDM4
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 21
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs353163
UBA6-AS1 ; TMPRSS11A
0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67 4
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2289519
SERPINB5
1.000 0.080 18 63493054 missense variant T/C snv 0.66 0.72 1
rs3213245
XRCC1 ; PINLYP
0.742 0.240 19 43575535 5 prime UTR variant G/A snv 0.65 0.60 13
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs2227981
LOC105373977 ; PDCD1
0.763 0.400 2 241851121 synonymous variant A/C;G snv 1.6E-04; 0.63 12
rs7813
GEMIN4
0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs7447927
STING1
1.000 0.080 5 139481561 synonymous variant C/G;T snv 0.62; 4.0E-06 1
rs7144658
TTC6 ; FOXA1
0.882 0.120 14 37592537 missense variant C/G;T snv 0.62 3
rs1126667
ALOX12 ; ALOX12-AS1
0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs238406
ERCC2
0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs9856
XIAP
0.925 0.120 X 123911791 3 prime UTR variant C/T snv 0.57 4
rs1494961
HELQ
0.925 0.160 4 83453327 missense variant C/T snv 0.56 0.60 3
rs11203366
PADI4
0.925 0.200 1 17331039 missense variant G/A snv 0.56 0.55 2
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1805034
TNFRSF11A
0.742 0.360 18 62360008 missense variant C/T snv 0.54 0.56 12