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rs62638197

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs62638197(C;T)
Make rs62638197(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position178994808
GeneGRM6
is asnp
is mentioned by
dbSNPrs62638197
ebirs62638197
HLIrs62638197
Exacrs62638197
Varsomers62638197
Maprs62638197
PheGenIrs62638197
hapmaprs62638197
1000 genomesrs62638197
hgdprs62638197
ensemblrs62638197
gopubmedrs62638197
geneviewrs62638197
scholarrs62638197
googlers62638197
pharmgkbrs62638197
gwascentralrs62638197
openSNPrs62638197
23andMers62638197
23andMe allrs62638197
SNP Nexus

SNPshotrs62638197
SNPdbers62638197
MSV3drs62638197
GWAS Ctlgrs62638197
Max Magnitude0
OMIM604096
Desc
Variant0005
Relatedalso
ClinVar
Risk rs62638197(T;T)
Alt rs62638197(T;T)
Reference rs62638197(C;C)
Significance Pathogenic
Disease Congenital stationary night blindness not provided
Variation info
Gene GRM6
CLNDBN Congenital stationary night blindness, type 1B not provided
Reversed 1
HGVS NC_000005.9:g.178421809G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006201.4, RCV000086025.1,