Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs2066713
SLC6A4
0.807 0.200 17 30224647 intron variant G/A snv 0.34 9
rs2498804
LOC102723342 ; SIVA1 ; LOC107987209
0.827 0.160 14 104766758 intron variant C/A;T snv 0.40 0.33 8
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 8
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs4251417
SLC6A4
0.827 0.200 17 30224840 intron variant C/T snv 6.8E-02 7
rs4500567
TSPAN8
0.807 0.200 12 71166082 intron variant G/A;C snv 6
rs7597593
ZNF804A
0.827 0.160 2 184668853 intron variant T/C snv 0.53 6
rs1705236
TSPAN8
0.827 0.200 12 71151778 intron variant T/A snv 7.6E-02 5
rs2279709
SLC18A1
0.882 0.120 8 20178722 intron variant T/G snv 0.51 5
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs2709370 0.851 0.120 2 207517878 intron variant A/C snv 0.17 4
rs10947563
FKBP5
0.925 0.040 6 35685660 intron variant G/A snv 0.77 3
rs12290811
TENM4
0.882 0.120 11 79372576 intron variant T/A snv 0.18 3
rs12701020
CRHR2
0.925 0.040 7 30655345 intron variant C/T snv 0.12 3
rs2546620
GABRB2
0.882 0.120 5 161332120 intron variant T/C snv 0.15 3
rs3798347
FKBP5 ; LOC112267956
0.925 0.040 6 35633999 intron variant A/T snv 0.65 3