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

rs62638208

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62638208(A;A)
Make rs62638208(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position178986689
GeneGRM6
is asnp
is mentioned by
dbSNPrs62638208
ebirs62638208
HLIrs62638208
Exacrs62638208
Varsomers62638208
Maprs62638208
PheGenIrs62638208
hapmaprs62638208
1000 genomesrs62638208
hgdprs62638208
ensemblrs62638208
gopubmedrs62638208
geneviewrs62638208
scholarrs62638208
googlers62638208
pharmgkbrs62638208
gwascentralrs62638208
openSNPrs62638208
23andMers62638208
23andMe allrs62638208
SNP Nexus

SNPshotrs62638208
SNPdbers62638208
MSV3drs62638208
GWAS Ctlgrs62638208
Max Magnitude0
OMIM604096
Desc
Variant0007
Relatedalso


ClinVar
Risk rs62638208(A;A)
Alt rs62638208(A;A)
Reference rs62638208(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.178413690C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006203.3, RCV000086028.1,