Gene: ARNTL ×
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: 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: 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: 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: rs1481892
rs1481892
ARNTL
3 11 13280374 intron variant G/C snv 0.62 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: rs3789327
rs3789327
ARNTL
6 0.925 0.080 11 13363769 intron variant A/G snv 0.53 0.010 1.000 1 2014 2014