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rs62637027

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs62637027(AA;AA)
Make rs62637027(AA;GC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position41474012
GeneNYX
is asnp
is mentioned by
dbSNPrs62637027
ebirs62637027
HLIrs62637027
Exacrs62637027
Varsomers62637027
Maprs62637027
PheGenIrs62637027
hapmaprs62637027
1000 genomesrs62637027
hgdprs62637027
ensemblrs62637027
gopubmedrs62637027
geneviewrs62637027
scholarrs62637027
googlers62637027
pharmgkbrs62637027
gwascentralrs62637027
openSNPrs62637027
23andMers62637027
23andMe allrs62637027
SNP Nexus

SNPshotrs62637027
SNPdbers62637027
MSV3drs62637027
GWAS Ctlgrs62637027
Max Magnitude0
OMIM300278
Desc
Variant0004
Relatedalso
ClinVar
Risk rs62637027(AA;AA)
Alt rs62637027(AA;AA)
Reference rs62637027(GC;GC)
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.41333265_41333266delGCinsAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000012176.11, RCV000086268.1,