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rs62638624

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs62638624(C;T)
Make rs62638624(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position178986132
GeneGRM6
is asnp
is mentioned by
dbSNPrs62638624
ebirs62638624
HLIrs62638624
Exacrs62638624
Varsomers62638624
Maprs62638624
PheGenIrs62638624
hapmaprs62638624
1000 genomesrs62638624
hgdprs62638624
ensemblrs62638624
gopubmedrs62638624
geneviewrs62638624
scholarrs62638624
googlers62638624
pharmgkbrs62638624
gwascentralrs62638624
openSNPrs62638624
23andMers62638624
23andMe allrs62638624
SNP Nexus

SNPshotrs62638624
SNPdbers62638624
MSV3drs62638624
GWAS Ctlgrs62638624
Max Magnitude0
OMIM604096
Desc
Variant0003
Relatedalso


ClinVar
Risk rs62638624(T;T)
Alt rs62638624(T;T)
Reference rs62638624(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.178413133G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006199.3, RCV000086044.1,