Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1137070
MAOA
0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs686
DRD1
0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs130058
HTR1B ; LOC105377864
0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs1042114
OPRD1
0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs751416416
OPRK1
0.882 0.120 8 53250920 missense variant C/A;T snv 8.3E-06; 4.1E-06 5
rs2910709
GDNF-AS1
0.882 0.120 5 37811762 non coding transcript exon variant A/G;T snv 4
rs11030096
BDNF-AS
0.925 0.160 11 27643996 intron variant T/A;C snv 3
rs265981
DRD1
0.925 0.080 5 175443899 5 prime UTR variant A/G;T snv 3
rs1022563
PDYN-AS1
0.925 0.080 20 1973693 intron variant C/G;T snv 2
rs1389752
MPDZ
0.925 0.080 9 13235288 intron variant A/G;T snv 2
rs1530351
RGS9
0.925 0.080 17 65135491 intron variant G/A;C snv 2
rs16917234
BDNF ; BDNF-AS
0.925 0.080 11 27676827 intron variant T/A;C snv 2
rs6556547
GABRB2
0.925 0.080 5 161333168 intron variant C/A;T snv 2
rs988712
BDNF-AS
0.925 0.160 11 27541835 intron variant G/A;T snv 2
rs1122079
RGS9
1.000 0.080 17 65218385 intron variant A/C;T snv 1
rs1714984
MYOCD
1.000 0.080 17 12714384 intron variant A/G;T snv 1
rs2270162
AUTS2 ; CT66
1.000 0.080 7 69596980 intron variant C/G;T snv 1
rs2288156
CCDC42
1.000 0.080 17 8741536 missense variant C/A;T snv 4.0E-06; 8.8E-02 1
rs274618
GRM3
1.000 0.080 7 86642700 upstream gene variant T/A;C snv 1
rs3219790
GRIN2A
1.000 0.080 16 10183568 upstream gene variant CACACACACACACACACA/-;CA;CACA;CACACA;CACACACA;CACACACACA;CACACACACACA;CACACACACACACA;CACACACACACACACA;CACACACACACACACACACA;CACACACACACACACACACACA;CACACACACACACACACACACACA;CACACACACACACACACACACACACA;CACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACACA;CACACACACACACACACACACACACACACACACACACACACA delins 1
rs4648319
DRD2
1.000 0.080 11 113443641 intron variant G/A;T snv 1