Have questions? Visit https://www.reddit.com/r/SNPedia

rs62638625

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62638625(A;A)
Make rs62638625(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position178983005
GeneGRM6
is asnp
is mentioned by
dbSNPrs62638625
ebirs62638625
HLIrs62638625
Exacrs62638625
Varsomers62638625
Maprs62638625
PheGenIrs62638625
hapmaprs62638625
1000 genomesrs62638625
hgdprs62638625
ensemblrs62638625
gopubmedrs62638625
geneviewrs62638625
scholarrs62638625
googlers62638625
pharmgkbrs62638625
gwascentralrs62638625
openSNPrs62638625
23andMers62638625
23andMe allrs62638625
SNP Nexus

SNPshotrs62638625
SNPdbers62638625
MSV3drs62638625
GWAS Ctlgrs62638625
Max Magnitude0
OMIM604096
Desc
Variant0002
Relatedalso


ClinVar
Risk rs62638625(A;A)
Alt rs62638625(A;A)
Reference rs62638625(G;G)
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.178410006C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006198.3, RCV000086047.1,