Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9557321
LOC101927437 ; CLYBL
1.000 0.120 13 99868847 intron variant T/C snv 3.8E-02 1
rs11761528
ZKSCAN5
1.000 0.120 7 99521178 intron variant C/T snv 0.12 4
rs372329931
ADH7
1.000 0.120 4 99435310 5 prime UTR variant T/C snv 4.3E-04 3.6E-04 2
rs740160
ARPC1A
1.000 0.120 7 99360257 intron variant C/T snv 8.6E-02 2
rs337527
GABBR2
1.000 0.120 9 98685681 intron variant T/C snv 3.9E-02 1
rs111988552
TSPAN5
1.000 0.120 4 98557163 intron variant A/T snv 1
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs746702110
OGG1
0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs3219008
OGG1
1.000 0.120 3 9753859 intron variant A/G snv 0.28 1
rs159153
OGG1 ; BRPF1
1.000 0.120 3 9748191 upstream gene variant T/C snv 0.32 1
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs2274795
PAPOLA
1.000 0.120 14 96528345 intron variant T/C snv 0.26 1
rs10520789 1.000 0.120 15 95598638 regulatory region variant G/A snv 0.12 1
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs3765534
ABCC4
0.882 0.200 13 95163161 missense variant C/T snv 2.3E-02 1.2E-02 4
rs11121380
SPSB1
1.000 0.120 1 9348900 intron variant A/C snv 0.11 1
rs42041
CDK6
0.882 0.280 7 92617430 intron variant C/G snv 0.21 3
rs4272
CDK6
1.000 0.120 7 92607515 3 prime UTR variant A/G;T snv 3
rs9909240
LOC105371532 ; NTN1
1.000 0.120 17 9236774 intron variant G/A snv 0.50 1
rs9516053
GPC5
1.000 0.120 13 92293631 intron variant T/A;C snv 1
rs7164176 1.000 0.120 15 91668544 intergenic variant G/A snv 0.65 1
rs284515 1.000 0.120 6 90499109 intergenic variant A/G snv 0.12 1
rs284511 1.000 0.120 6 90498823 intergenic variant T/A;C snv 1