Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1481892
ARNTL
11 13280374 intron variant G/C snv 0.62 3
rs35275025
PER1
1.000 0.080 17 8141219 missense variant C/G;T snv 4.0E-06 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
rs9315202 0.925 0.080 13 33067879 downstream gene variant C/T snv 0.24 4
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
rs9563121
KL
0.925 0.080 13 33050369 intron variant C/T snv 0.26 4
rs2640909
PER3
1 7830057 missense variant T/C snv 0.14 0.23 4
rs1229030855
TIMELESS
0.925 0.080 12 56428321 missense variant A/G;T snv 4.0E-06; 4.0E-06 4
rs137854602
SCN5A
0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 5
rs4719714
STEAP1B
1.000 0.080 7 22721094 intron variant A/T snv 0.21 5
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
rs11824092
ARNTL
0.925 0.080 11 13324747 intron variant T/C snv 0.62 7
rs1044397
CHRNA4
0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 7
rs1212171
NTRK2
0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 8
rs738499
TEF ; LOC105373042
0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs1481318368
TH
0.827 0.120 11 2169802 missense variant C/T snv 10
rs767181086
LAMC2
0.827 0.240 1 183220922 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs61751362
MECP2
0.790 0.160 X 154030948 stop gained G/A;C snv 1.6E-05 14