Disease: Mental disorders
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2
rs2044117
NALCN ; NALCN-AS1
13 101055958 intron variant G/A snv 0.19 2
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs4996815 13 105999312 intron variant G/T snv 0.61 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 2
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs11789407
LOC105376249
9 118597268 intergenic variant C/A snv 0.44 2
rs10496702
NCKAP5
2 133247997 intron variant G/A snv 0.18 2
rs7600871
NCKAP5
2 133257389 intron variant C/T snv 0.16 2
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2
rs802524
CNTNAP2
7 146254550 intron variant T/C;G snv 2
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs6444931
CLDN11
3 170445686 intron variant G/A snv 0.85 2
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4