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
rs10083466
NRXN3
1.000 0.040 14 79518375 intron variant C/A snv 0.39 1
rs10947563
FKBP5
0.925 0.040 6 35685660 intron variant G/A snv 0.77 3
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs11199993
FGFR2
0.925 0.120 10 121531750 intron variant G/C snv 4.8E-02 2
rs1128306
HCG9 ; HLA-A
0.925 0.120 6 29975492 non coding transcript exon variant G/A snv 0.22 2
rs113507694
DPPA3
1.000 0.040 12 7714013 intron variant A/G snv 3.2E-02 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs12718541
FIGNL1 ; DDC
0.925 0.080 7 50482446 intron variant A/G snv 0.55 2
rs1311223100
SLC18A1
0.925 0.120 8 20180955 frameshift variant T/- del 5.2E-06 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs1390938
SLC18A1
0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs1497020
SLC18A1
0.925 0.120 8 20144915 3 prime UTR variant G/A snv 0.75 2
rs1610037
ADCYAP1
0.925 0.120 18 910634 3 prime UTR variant A/G snv 0.26 2
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1705236
TSPAN8
0.827 0.200 12 71151778 intron variant T/A snv 7.6E-02 5
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 14
rs175174
ZDHHC8
0.882 0.120 22 20140031 non coding transcript exon variant A/G snv 0.44 3
rs187269
GABRB2
0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs1938516
ERVMER61-1
0.925 0.120 1 187433789 intron variant T/A snv 5.7E-02 2
rs2066713
SLC6A4
0.807 0.200 17 30224647 intron variant G/A snv 0.34 9
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54