Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008492 1.000 0.120 4 38764099 intergenic variant C/G;T snv 2
rs1003421753
IL12A ; IL12A-AS1
1.000 0.120 3 159989088 missense variant C/T snv 1
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1039312028
BAX
1.000 0.120 19 48955724 missense variant G/A snv 1.4E-05 1
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1041163
VCAM1
0.882 0.160 1 100718269 upstream gene variant T/C snv 0.18 3
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1049216
CASP3
0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs1053667
TOGARAM1
0.925 0.120 14 45073835 3 prime UTR variant T/C snv 0.11 4
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs11038689
CRY2
0.882 0.160 11 45852713 intron variant A/G snv 0.19 3
rs1127717
ALDH1L1-AS1 ; ALDH1L1
0.925 0.160 3 126107216 missense variant T/C snv 0.18 0.20 3
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11337
GOLGA7
0.925 0.120 8 41510767 3 prime UTR variant T/G snv 0.93 4
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs113686495
CASP8
0.925 0.160 2 201258757 intron variant ATTCTGTC/- delins 4
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs114216685
RAD54B ; FSBP
1.000 0.120 8 94391640 missense variant T/C snv 8.8E-04 3.9E-04 1