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rs62637037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62637037(A;A)
Make rs62637037(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position41474502
GeneNYX
is asnp
is mentioned by
dbSNPrs62637037
ebirs62637037
HLIrs62637037
Exacrs62637037
Varsomers62637037
Maprs62637037
PheGenIrs62637037
hapmaprs62637037
1000 genomesrs62637037
hgdprs62637037
ensemblrs62637037
gopubmedrs62637037
geneviewrs62637037
scholarrs62637037
googlers62637037
pharmgkbrs62637037
gwascentralrs62637037
openSNPrs62637037
23andMers62637037
23andMe allrs62637037
SNP Nexus

SNPshotrs62637037
SNPdbers62637037
MSV3drs62637037
GWAS Ctlgrs62637037
Max Magnitude0
OMIM300278
Desc
Variant0002
Relatedalso


ClinVar
Risk rs62637037(A;A)
Alt rs62637037(A;A)
Reference rs62637037(G;G)
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.41333755G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012174.11, RCV000086260.1,