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rs121434304

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434304(C;C)
Make rs121434304(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position178989075
GeneGRM6
is asnp
is mentioned by
dbSNPrs121434304
ebirs121434304
HLIrs121434304
Exacrs121434304
Varsomers121434304
Maprs121434304
PheGenIrs121434304
hapmaprs121434304
1000 genomesrs121434304
hgdprs121434304
ensemblrs121434304
gopubmedrs121434304
geneviewrs121434304
scholarrs121434304
googlers121434304
pharmgkbrs121434304
gwascentralrs121434304
openSNPrs121434304
23andMers121434304
23andMe allrs121434304
SNP Nexus

SNPshotrs121434304
SNPdbers121434304
MSV3drs121434304
GWAS Ctlgrs121434304
Max Magnitude0
OMIM604096
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121434304(C;C)
Alt rs121434304(C;C)
Reference rs121434304(T;T)
Significance Other
Disease Congenital stationary night blindness
Variation info
Gene GRM6
CLNDBN Congenital stationary night blindness, type 1B
Reversed 1
HGVS NC_000005.9:g.178416076A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006204.4,