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rs62637021

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs62637021(A;A)
Make rs62637021(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position41473558
GeneNYX
is asnp
is mentioned by
dbSNPrs62637021
ebirs62637021
HLIrs62637021
Exacrs62637021
Varsomers62637021
Maprs62637021
PheGenIrs62637021
hapmaprs62637021
1000 genomesrs62637021
hgdprs62637021
ensemblrs62637021
gopubmedrs62637021
geneviewrs62637021
scholarrs62637021
googlers62637021
pharmgkbrs62637021
gwascentralrs62637021
openSNPrs62637021
23andMers62637021
23andMe allrs62637021
SNP Nexus

SNPshotrs62637021
SNPdbers62637021
MSV3drs62637021
GWAS Ctlgrs62637021
Max Magnitude0
OMIM300278
Desc
Variant0003
Relatedalso


ClinVar
Risk rs62637021(A;A)
Alt rs62637021(A;A)
Reference rs62637021(C;C)
Significance Pathogenic
Disease Congenital stationary night blindness not provided
Variation info
Gene NYX
CLNDBN Congenital stationary night blindness, type 1A not provided
Reversed 0
HGVS NC_000023.10:g.41332811C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012175.17, RCV000086261.1,