Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs4151667
CFB ; CYP21A2
0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 9
rs1923884
HTR2A
1.000 0.120 13 46847701 intron variant C/T snv 0.12 2
rs11214105
TEX12 ; LOC107987164
1.000 0.120 11 112166930 intron variant G/A snv 0.25 2
rs2247215
GRIK2
1.000 0.120 6 101518578 intron variant A/G snv 0.26 1
rs369729113
HTR5A ; HTR5A-AS1
1.000 0.120 7 155071001 synonymous variant C/G;T snv 2.0E-05 1
rs1205738080
HTR7
1.000 0.120 10 90857570 synonymous variant G/A snv 4.9E-06 1
rs356653
NPAS2
1.000 0.120 2 100923328 intron variant G/A;C snv 0.36 1