Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10798059
PLA2G4A
0.925 0.080 1 186830478 intron variant G/A snv 0.40 2
rs2072660
CHRNB2
1.000 0.080 1 154576245 3 prime UTR variant T/C;G snv 1
rs4845652
LOC107985206
1.000 0.080 1 154565729 non coding transcript exon variant C/A;T snv 1
rs10865246
NRXN1
1.000 0.080 2 50443116 intron variant C/A;T snv 1
rs12466358
CHRND
1.000 0.080 2 232532815 intron variant T/G snv 0.22 1
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1486012 0.925 0.080 3 114120575 intergenic variant A/T snv 0.53 2
rs2399496
DRD3
0.925 0.080 3 114127166 downstream gene variant T/A snv 0.45 2
rs963468
DRD3
0.925 0.080 3 114144040 intron variant G/A snv 0.30 2
rs2878298
RHOA
1.000 0.080 3 49368647 intron variant T/C snv 0.43 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1573496
ADH7
0.827 0.160 4 99428512 missense variant C/G snv 8.5E-02; 4.9E-04 7.8E-02 7
rs4425326
NPY2R
0.925 0.080 4 155186084 intron variant C/T snv 0.47 2
rs4861065
CHRNA9
1.000 0.080 4 40342378 intron variant T/C snv 0.32 1
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs6198
NR3C1
0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 10
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs4532
DRD1
0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs378042
STARD4-AS1 ; LOC105369177
1.000 0.080 5 111524099 intron variant G/A snv 1
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95