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: rs10838524
rs10838524
CRY2
5 0.851 0.120 11 45848626 intron variant A/G snv 0.42 0.010 1.000 1 2012 2012
dbSNP: rs11541353
rs11541353
NPAS2 ; NPAS2-AS1
4 0.851 0.120 2 100977729 missense variant C/T snv 0.14 0.14 0.010 1.000 1 2012 2012
dbSNP: rs2028122
rs2028122
RORA ; RORA-AS1
4 0.851 0.120 15 60549076 intron variant A/G snv 0.51 0.010 1.000 1 2012 2012
dbSNP: rs2287161
rs2287161
MTERF2
7 0.827 0.080 12 106987362 upstream gene variant C/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs2314339
rs2314339
NR1D1
4 0.851 0.120 17 40096959 intron variant C/T snv 0.20 0.010 1.000 1 2012 2012