Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 7
rs1799913
TPH1
0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 5
rs2306073
ARNTL2 ; ARNTL2-AS1
0.882 0.080 12 27402904 intron variant C/T snv 0.37 4
rs3782025
HTR3B
0.882 0.080 11 113936885 intron variant G/A snv 0.55 4
rs463379
SLC6A3
0.882 0.080 5 1431049 intron variant G/C snv 0.31 3
rs4964057
ARNTL2
0.882 0.080 12 27363909 intron variant T/G snv 0.29 3
rs6350
SLC6A3
0.882 0.080 5 1443084 missense variant G/A;C snv 5.6E-02; 6.8E-05 3
rs11240
CLOCK ; TMEM165
0.925 0.080 4 55453183 3 prime UTR variant C/A;G snv 2
rs11941860
GABRG1
1.000 0.080 4 46080161 intron variant C/T snv 0.12 2
rs2119183
GABRA2
1.000 0.080 4 46270789 intron variant G/A snv 7.6E-02 2
rs2836016
KCNJ6
0.925 0.080 21 37840718 intron variant G/A snv 0.59 0.58 2
rs3756007
GABRA2
1.000 0.080 4 46389047 5 prime UTR variant T/C snv 5.4E-02 2
rs3811939
CRHBP
1.000 0.080 5 76954762 intron variant G/A snv 0.27 2
rs536599 1.000 0.080 4 46196917 intergenic variant G/T snv 0.47 2
rs56013859
PER2
0.925 0.080 2 238276865 intron variant T/C snv 0.11 2
rs6473797
OPRK1
0.925 0.080 8 53240422 intron variant T/C snv 0.39 2
rs10044881
HTR4
1.000 0.080 5 148645656 non coding transcript exon variant T/C snv 0.17 1
rs10405681
PIP5K1C
1.000 0.080 19 3634021 intron variant C/A;T snv 1
rs10419980
PIP5K1C
1.000 0.080 19 3685118 intron variant C/T snv 0.29 1
rs10432303
PIP5K1C
1.000 0.080 19 3656654 intron variant G/A snv 0.41 1
rs11250159
GATA4
1.000 0.080 8 11729725 intron variant G/A;T snv 1
rs141973904
ADH1B ; ADH1C
1.000 0.080 4 99341085 intron variant C/T snv 1.6E-02 1
rs1476592
PIP5K1C
1.000 0.080 19 3679742 intron variant A/G;T snv 1