Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs7958822
ARNTL2
0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 5
rs17153694
GATA4
0.851 0.160 8 11730972 intron variant C/T snv 0.12 4
rs2306073
ARNTL2 ; ARNTL2-AS1
0.882 0.080 12 27402904 intron variant C/T snv 0.37 4
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs3782025
HTR3B
0.882 0.080 11 113936885 intron variant G/A snv 0.55 4
rs10112596
GATA4
0.925 0.120 8 11722293 intron variant A/G snv 0.83 3
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
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
rs3811939
CRHBP
1.000 0.080 5 76954762 intron variant G/A snv 0.27 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
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
rs17777298
LOC107986462 ; HTR4
1.000 0.080 5 148541962 intron variant T/A snv 0.24 1