Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs10766075
ARNTL
0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs1082214
MIP
0.925 0.080 12 56452706 non coding transcript exon variant C/T snv 9.3E-02 6
rs11022778
ARNTL
0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 6
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs2291739
TIMELESS
0.925 0.080 12 56420869 missense variant G/A;C snv 0.49; 4.0E-06 6
rs3789327
ARNTL
0.925 0.080 11 13363769 intron variant A/G snv 0.53 6
rs12936511
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
0.925 0.080 17 45807036 synonymous variant C/T snv 3.1E-02 3.0E-02 5
rs1415259
NOS1AP ; LOC105371475
0.925 0.080 1 162115519 intron variant C/T snv 0.54 5
rs10988134
KYAT1 ; SPOUT1
0.925 0.080 9 128833128 3 prime UTR variant C/T snv 0.34 4
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs115482041
RCL1
0.925 0.080 9 4860267 missense variant C/T snv 2.6E-03 2.3E-03 4
rs1491851 0.925 0.080 11 27731216 intron variant T/C;G snv 0.41 4
rs1800035
ADRA2A
0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 4
rs3125
HTR2A
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv 4
rs36010656
SLCO1C1
0.925 0.080 12 20711408 missense variant C/A;T snv 3.4E-02 4
rs10510057 0.925 0.080 10 119551536 intergenic variant G/C snv 0.22 3
rs10997871
SIRT1
0.925 0.080 10 67913178 intron variant T/C snv 4.1E-03 3
rs1187329
NTRK2
0.925 0.080 9 84674365 intron variant A/G snv 0.52 3
rs12137417
TSNAX-DISC1 ; DISC1
0.925 0.080 1 231950407 intron variant G/A snv 0.17 3
rs12229394
TPH2
0.925 0.080 12 71999134 intron variant G/A snv 0.29 3
rs1364647619
POMC
0.925 0.080 2 25161334 missense variant C/T snv 3
rs139832701
CAV3
0.925 0.080 3 8773124 intron variant T/G snv 0.13 3
rs174696
COMT
0.925 0.080 22 19965653 intron variant C/A;T snv 3