Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 46
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs61751362
MECP2
0.790 0.160 X 154030948 stop gained G/A;C snv 1.6E-05 14
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs738499
TEF ; LOC105373042
0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs10766075
ARNTL
0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs11022778
ARNTL
0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs3789327
ARNTL
0.925 0.080 11 13363769 intron variant A/G snv 0.53 6
rs2291739
TIMELESS
0.925 0.080 12 56420869 missense variant G/A;C snv 0.49; 4.0E-06 6
rs11600996
ARNTL
1.000 0.040 11 13374619 intron variant T/C snv 0.40 4
rs1982350
ARNTL
11 13328584 intron variant A/G snv 0.57 4
rs2640909
PER3
1 7830057 missense variant T/C snv 0.14 0.23 4
rs1481892
ARNTL
11 13280374 intron variant G/C snv 0.62 3
rs10864315
PER3
1 7790021 intron variant C/T snv 0.28 3
rs3805148
TMEM165 ; CLOCK
4 55440643 intron variant A/C snv 0.33 3