Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs1106634
ATP6V1B2
0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs11111
GDNF-AS1 ; GDNF
0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs115482041
RCL1
0.925 0.080 9 4860267 missense variant C/T snv 2.6E-03 2.3E-03 4
rs11636753
CHRNB4
0.882 0.120 15 78636604 intron variant G/T snv 0.35 4
rs1173546708
TPH1
0.851 0.120 11 18040661 synonymous variant G/A snv 4.0E-06 5
rs11754661
MTHFD1L
0.851 0.120 6 150885942 intron variant G/A;T snv 6
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs1187323
NTRK2
0.882 0.080 9 84668501 upstream gene variant C/A;G;T snv 5
rs1187329
NTRK2
0.925 0.080 9 84674365 intron variant A/G snv 0.52 3
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs11911834
S100B
0.882 0.080 21 46602608 5 prime UTR variant G/A;T snv 4
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs120074175
TPH2
0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 7
rs1202184
ABCB1
0.851 0.120 7 87584585 intron variant C/T snv 0.39 7
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1212171
NTRK2
0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs12137417
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231950407 intron variant G/A snv 0.17 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1220000453
ZFP91-CNTF ; CNTF
0.882 0.120 11 58624189 synonymous variant C/T snv 5
rs12229394
TPH2
0.925 0.080 12 71999134 intron variant G/A snv 0.29 3
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83