Source: CURATED

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 7
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs1057523354
COL4A1
0.763 0.480 13 110179387 missense variant C/A snv 13
rs1082214
MIP
0.925 0.080 12 56452706 non coding transcript exon variant C/T snv 9.3E-02 1
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 10
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 4
rs1106634
ATP6V1B2
0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 1
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 1
rs1131691771
PHIP ; IRAK1BP1
0.807 0.160 6 78958469 splice donor variant ACTT/- delins 18
rs11754661
MTHFD1L
0.851 0.120 6 150885942 intron variant G/A;T snv 1
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 1
rs120074175
TPH2
0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 1
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs12912233
RORA
0.851 0.120 15 60974897 intron variant C/T snv 0.38 1
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 1
rs139315125
PER3
0.851 0.080 1 7809900 missense variant A/G snv 5.6E-03 5.0E-03 1
rs1415259
NOS1AP ; LOC105371475
0.925 0.080 1 162115519 intron variant C/T snv 0.54 2
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 1
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 1
rs149729531
CLCN1
0.851 0.200 7 143321432 missense variant C/G snv 1.2E-03 7.5E-04 3
rs1545843
LOC107984536
0.827 0.120 12 84170289 intron variant G/A snv 0.52 1
rs1554887097
MRPL43 ; TWNK
0.807 0.320 10 100989331 missense variant G/A snv 10
rs1554888939
EHMT1
0.683 0.640 9 137798823 missense variant G/T snv 58