Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10432303
PIP5K1C
1.000 0.080 19 3656654 intron variant G/A snv 0.41 1
rs11250159
GATA4
1.000 0.080 8 11729725 intron variant G/A;T snv 1
rs141973904
ADH1B ; ADH1C
1.000 0.080 4 99341085 intron variant C/T snv 1.6E-02 1
rs1476592
PIP5K1C
1.000 0.080 19 3679742 intron variant A/G;T snv 1
rs17777298
LOC107986462 ; HTR4
1.000 0.080 5 148541962 intron variant T/A snv 0.24 1
rs4432372
PIP5K1C
1.000 0.080 19 3698844 intron variant A/G;T snv 1
rs4807493
PIP5K1C
1.000 0.080 19 3631038 3 prime UTR variant A/G snv 0.84 1
rs6990313
GATA4
1.000 0.080 8 11712527 intron variant G/T snv 0.14 1
rs8109485
PIP5K1C
1.000 0.080 19 3664096 intron variant A/G snv 0.21 1
rs916264
APOL2
1.000 0.080 22 36237790 intron variant A/C;T snv 1
rs1015443
PRH1-PRR4 ; PRR4 ; TAS2R13 ; PRH1
0.925 0.160 12 10908523 missense variant T/A;C snv 4.0E-06; 0.59 2
rs6923761
GLP1R
0.851 0.200 6 39066296 missense variant G/A;C snv 0.23; 4.0E-06 4
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2074957
PIP5K1C
1.000 0.080 19 3653527 synonymous variant C/A;T snv 8.0E-06; 0.57 1
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6350
SLC6A3
0.882 0.080 5 1443084 missense variant G/A;C snv 5.6E-02; 6.8E-05 3
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 7
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1799913
TPH1
0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249