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rs61755817

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61755817(C;C)
Make rs61755817(C;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position42704457
GeneLOC101929618, PRPH2
is asnp
is mentioned by
dbSNPrs61755817
ebirs61755817
HLIrs61755817
Exacrs61755817
Varsomers61755817
Maprs61755817
PheGenIrs61755817
hapmaprs61755817
1000 genomesrs61755817
hgdprs61755817
ensemblrs61755817
gopubmedrs61755817
geneviewrs61755817
scholarrs61755817
googlers61755817
pharmgkbrs61755817
gwascentralrs61755817
openSNPrs61755817
23andMers61755817
23andMe allrs61755817
SNP Nexus

SNPshotrs61755817
SNPdbers61755817
MSV3drs61755817
GWAS Ctlgrs61755817
Max Magnitude0


ClinVar
Risk rs61755817(C;C)
Alt rs61755817(C;C)
Reference rs61755817(T;T)
Significance Pathogenic
Disease not provided Retinitis pigmentosa
Variation info
Gene PRPH2
CLNDBN not provided Retinitis pigmentosa
Reversed 1
HGVS NC_000006.11:g.42672195A>G
CLNSRC ClinVar Retina International
CLNACC RCV000085019.1, RCV000132580.1,