Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1432441
MAP2K1
0.882 0.040 15 66426943 intron variant G/A snv 0.27 3
rs1549854
MAP2K1
0.882 0.040 15 66404397 intron variant A/C;G snv 0.44 3
rs12256138
SLC29A3
1.000 0.040 10 71336479 intron variant C/G;T snv 1
rs7182853
MAP2K1
1.000 0.040 15 66469947 intron variant T/C snv 0.31 1
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs2242446
SLC6A2
0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs120074175
TPH2
0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 7
rs139315125
PER3
0.851 0.080 1 7809900 missense variant A/G snv 5.6E-03 5.0E-03 7
rs2072621
GPR50-AS1 ; GPR50
0.851 0.080 X 151177387 non coding transcript exon variant C/A;G snv 7
rs2268498
CAV3 ; OXTR
0.827 0.080 3 8770725 intron variant T/C snv 0.41 7
rs2287161
MTERF2
0.827 0.080 12 106987362 upstream gene variant C/G;T snv 7
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
rs57875989
PER3
0.882 0.080 1 7829913 splice acceptor variant GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC/-;GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGCGCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC delins 0.11 0.18 7
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 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
rs1409851868
EPHA3
0.882 0.080 3 89399325 missense variant 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
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs2291739
TIMELESS
0.925 0.080 12 56420869 missense variant G/A;C snv 0.49; 4.0E-06 6