Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 7
rs7958822
ARNTL2
0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs3782025
HTR3B
0.882 0.080 11 113936885 intron variant G/A snv 0.55 4
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
rs10432303
PIP5K1C
1.000 0.080 19 3656654 intron variant G/A snv 0.41 1
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs6923761
GLP1R
0.851 0.200 6 39066296 missense variant G/A;C snv 0.23; 4.0E-06 4
rs6350
SLC6A3
0.882 0.080 5 1443084 missense variant G/A;C snv 5.6E-02; 6.8E-05 3
rs1799913
TPH1
0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs11250159
GATA4
1.000 0.080 8 11729725 intron variant G/A;T snv 1
rs463379
SLC6A3
0.882 0.080 5 1431049 intron variant G/C snv 0.31 3
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs536599 1.000 0.080 4 46196917 intergenic variant G/T snv 0.47 2
rs6990313
GATA4
1.000 0.080 8 11712527 intron variant G/T snv 0.14 1
rs17777298
LOC107986462 ; HTR4
1.000 0.080 5 148541962 intron variant T/A snv 0.24 1
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1015443
PRH1-PRR4 ; PRR4 ; TAS2R13 ; PRH1
0.925 0.160 12 10908523 missense variant T/A;C snv 4.0E-06; 0.59 2
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
rs356200
SNCA
0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs2412646
CLOCK ; TMEM165
0.882 0.120 4 55452605 3 prime UTR variant T/C snv 0.58 3
rs3756007
GABRA2
1.000 0.080 4 46389047 5 prime UTR variant T/C snv 5.4E-02 2
rs56013859
PER2
0.925 0.080 2 238276865 intron variant T/C snv 0.11 2