Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10112596
GATA4
0.925 0.120 8 11722293 intron variant A/G snv 0.83 3
rs1012176
CTNND2
5 11320426 intron variant G/T snv 0.24 1
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
rs10835210
BDNF ; BDNF-AS
0.882 0.040 11 27674363 intron variant C/A;G snv 4
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs10893268
OR8A1
11 124568716 intron variant C/T snv 0.40 1
rs11030107
BDNF ; BDNF-AS
1.000 0.040 11 27673288 intron variant A/G snv 0.19 2
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs11059336 12 127745489 regulatory region variant T/C snv 0.14 1
rs1110976
DRD2
1.000 0.040 11 113413797 intron variant T/G snv 3
rs11111
GDNF-AS1 ; GDNF
0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5
rs112146896
EFHD2
1.000 0.040 1 15418527 intron variant A/C;G;T snv 2
rs113209956 9 25211195 intergenic variant C/T snv 5.4E-02 1
rs1132358
BAIAP3
1.000 0.040 16 1347814 synonymous variant C/T snv 0.44 0.39 3
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs11669576
LDLR ; MIR6886
0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 6
rs1181732881
DLX4
17 49969496 missense variant G/A;C;T snv 1
rs11855560
RAD51
15 40732105 3 prime UTR variant T/C snv 0.49 1
rs1192553 1 17967858 intergenic variant G/A snv 0.70 1