Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10864315
rs10864315
PER3
3 1 7790021 intron variant C/T snv 0.28 0.010 1.000 1 2016 2016
dbSNP: rs1481892
rs1481892
ARNTL
3 11 13280374 intron variant G/C snv 0.62 0.010 1.000 1 2016 2016
dbSNP: rs35275025
rs35275025
PER1
3 1.000 0.080 17 8141219 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs3805148
rs3805148
CLOCK ; TMEM165
3 4 55440643 intron variant A/C snv 0.33 0.010 1.000 1 2016 2016
dbSNP: rs11600996
rs11600996
ARNTL
4 1.000 0.040 11 13374619 intron variant T/C snv 0.40 0.010 1.000 1 2016 2016
dbSNP: rs1229030855
rs1229030855
TIMELESS
4 0.925 0.080 12 56428321 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1982350
rs1982350
ARNTL
4 11 13328584 intron variant A/G snv 0.57 0.010 1.000 1 2016 2016
dbSNP: rs2640909
rs2640909
PER3
4 1 7830057 missense variant T/C snv 0.14 0.23 0.010 1.000 1 2016 2016
dbSNP: rs9315202
rs9315202 		4 0.925 0.080 13 33067879 downstream gene variant C/T snv 0.24 0.010 1.000 1 2019 2019
dbSNP: rs9563121
rs9563121
KL
4 0.925 0.080 13 33050369 intron variant C/T snv 0.26 0.010 1.000 1 2019 2019
dbSNP: rs137854602
rs137854602
SCN5A
5 0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 0.010 1.000 1 2016 2016
dbSNP: rs4719714
rs4719714
STEAP1B
5 1.000 0.080 7 22721094 intron variant A/T snv 0.21 0.010 1.000 1 2010 2010
dbSNP: rs10766075
rs10766075
ARNTL
6 0.925 0.080 11 13297040 intron variant C/T snv 0.27 0.010 1.000 1 2014 2014
dbSNP: rs11022778
rs11022778
ARNTL
6 0.925 0.080 11 13369313 intron variant T/A;G snv 0.010 1.000 1 2014 2014
dbSNP: rs156243
rs156243 		6 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 0.010 1.000 1 2014 2014
dbSNP: rs2291739
rs2291739
TIMELESS
6 0.925 0.080 12 56420869 missense variant G/A;C snv 0.49; 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs3789327
rs3789327
ARNTL
6 0.925 0.080 11 13363769 intron variant A/G snv 0.53 0.010 1.000 1 2014 2014
dbSNP: rs11824092
rs11824092
ARNTL
7 0.925 0.080 11 13324747 intron variant T/C snv 0.62 0.020 1.000 2 2014 2016
dbSNP: rs1044397
rs1044397
CHRNA4
7 0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 0.010 1.000 1 2015 2015
dbSNP: rs1212171
rs1212171
NTRK2
8 0.851 0.120 9 84667612 upstream gene variant C/T snv 0.50 0.010 1.000 1 2017 2017
dbSNP: rs738499
rs738499
TEF ; LOC105373042
9 0.851 0.120 22 41381096 intron variant G/T snv 0.76 0.010 1.000 1 2012 2012
dbSNP: rs1481318368
rs1481318368
TH
10 0.827 0.120 11 2169802 missense variant C/T snv 0.010 1.000 1 2013 2013
dbSNP: rs767181086
rs767181086
LAMC2
11 0.827 0.240 1 183220922 stop gained G/A;T snv 8.0E-06; 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs11932595
rs11932595
CLOCK
12 0.827 0.160 4 55457430 intron variant A/G;T snv 0.020 1.000 2 2014 2016
dbSNP: rs61751362
rs61751362
MECP2
14 0.790 0.160 X 154030948 stop gained G/A;C snv 1.6E-05 0.010 1.000 1 2016 2016