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
rs11600996
ARNTL
1.000 0.040 11 13374619 intron variant T/C snv 0.40 4
rs2640909
PER3
1 7830057 missense variant T/C snv 0.14 0.23 4
rs11022778
ARNTL
0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs738499
TEF ; LOC105373042
0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs1481892
ARNTL
11 13280374 intron variant G/C snv 0.62 3
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs767181086
LAMC2
0.827 0.240 1 183220922 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs61751362
MECP2
0.790 0.160 X 154030948 stop gained G/A;C snv 1.6E-05 14
rs2291739
TIMELESS
0.925 0.080 12 56420869 missense variant G/A;C snv 0.49; 4.0E-06 6
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 46
rs28933385
PRNP
0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs137854602
SCN5A
0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 5
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs1212171
NTRK2
0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs1044397
CHRNA4
0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 7
rs10766075
ARNTL
0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs9315202 0.925 0.080 13 33067879 downstream gene variant C/T snv 0.24 4
rs9563121
KL
0.925 0.080 13 33050369 intron variant C/T snv 0.26 4