Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6990313
GATA4
1.000 0.080 8 11712527 intron variant G/T snv 0.14 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs10044881
HTR4
1.000 0.080 5 148645656 non coding transcript exon variant T/C snv 0.17 1
rs8109485
PIP5K1C
1.000 0.080 19 3664096 intron variant A/G snv 0.21 1
rs17777298
LOC107986462 ; HTR4
1.000 0.080 5 148541962 intron variant T/A snv 0.24 1
rs3811939
CRHBP
1.000 0.080 5 76954762 intron variant G/A snv 0.27 2
rs4964057
ARNTL2
0.882 0.080 12 27363909 intron variant T/G snv 0.29 3
rs10419980
PIP5K1C
1.000 0.080 19 3685118 intron variant C/T snv 0.29 1
rs463379
SLC6A3
0.882 0.080 5 1431049 intron variant G/C snv 0.31 3
rs1799913
TPH1
0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs2306073
ARNTL2 ; ARNTL2-AS1
0.882 0.080 12 27402904 intron variant C/T snv 0.37 4
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 5
rs6473797
OPRK1
0.925 0.080 8 53240422 intron variant T/C snv 0.39 2
rs10432303
PIP5K1C
1.000 0.080 19 3656654 intron variant G/A snv 0.41 1
rs7958822
ARNTL2
0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs536599 1.000 0.080 4 46196917 intergenic variant G/T snv 0.47 2
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs356219
LOC105377329 ; SNCA
0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs3782025
HTR3B
0.882 0.080 11 113936885 intron variant G/A snv 0.55 4
rs2412646
CLOCK ; TMEM165
0.882 0.120 4 55452605 3 prime UTR variant T/C snv 0.58 3
rs2836016
KCNJ6
0.925 0.080 21 37840718 intron variant G/A snv 0.59 0.58 2
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193