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rs62638202

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62638202(A;A)
Make rs62638202(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position178994497
GeneGRM6
is asnp
is mentioned by
dbSNPrs62638202
ebirs62638202
HLIrs62638202
Exacrs62638202
Varsomers62638202
Maprs62638202
PheGenIrs62638202
hapmaprs62638202
1000 genomesrs62638202
hgdprs62638202
ensemblrs62638202
gopubmedrs62638202
geneviewrs62638202
scholarrs62638202
googlers62638202
pharmgkbrs62638202
gwascentralrs62638202
openSNPrs62638202
23andMers62638202
23andMe allrs62638202
SNP Nexus

SNPshotrs62638202
SNPdbers62638202
MSV3drs62638202
GWAS Ctlgrs62638202
Max Magnitude0
OMIM604096
Desc
Variant0004
Relatedalso


ClinVar
Risk rs62638202(A;A)
Alt rs62638202(A;A)
Reference rs62638202(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.178421498C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006200.3, RCV000086056.1,