Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7486220
TIMELESS
0.925 0.080 12 56443632 intron variant C/T snv 3
rs12229394
TPH2
0.925 0.080 12 71999134 intron variant G/A snv 0.29 3
rs12137417
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231950407 intron variant G/A snv 0.17 3
rs2793094
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231741236 intron variant G/A snv 0.97 3
rs10997875 0.882 0.080 10 67920067 downstream gene variant T/A;C snv 4
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs1491851 0.925 0.080 11 27731216 intron variant T/C;G snv 0.41 4
rs4305745 0.882 0.080 6 132572573 downstream gene variant G/A snv 0.55 4
rs7452939 0.882 0.080 6 132572626 downstream gene variant G/A snv 4
rs143830698
ACE
0.882 0.120 17 63488659 missense variant G/A snv 8.4E-05 4
rs769397961
ACE
0.882 0.120 17 63488758 missense variant G/A snv 1.2E-05 3.5E-05 4
rs1863918
ADAMTS2
0.882 0.160 5 179112381 3 prime UTR variant G/T snv 0.25 4
rs2228079
ADORA1
0.882 0.160 1 203129147 synonymous variant T/G snv 0.31 0.26 4
rs1800035
ADRA2A
0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 4
rs10848635
CACNA1C
0.882 0.080 12 2207029 intron variant T/A;C snv 0.34 4
rs772659997
CHAT
0.882 0.120 10 49619853 synonymous variant T/C snv 2.0E-05 4
rs11636753
CHRNB4
0.882 0.120 15 78636604 intron variant G/T snv 0.35 4
rs1876828
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.851 0.160 17 45834159 intron variant C/T snv 0.14 4
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs760761
DTNBP1
0.882 0.080 6 15650901 intron variant G/A snv 0.26 4
rs4672619
ERBB4
0.882 0.160 2 211592470 intron variant C/A;G snv 4
rs2910709
GDNF-AS1
0.882 0.120 5 37811762 non coding transcript exon variant A/G;T snv 4
rs561077
GPR50
0.882 0.080 X 151181177 missense variant A/G snv 0.43 0.45 4
rs1800041
HTR1A
0.882 0.120 5 63961673 missense variant G/A snv 1.8E-03 5.3E-04 4
rs3125
HTR2A
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv 4