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rs61755794

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61755794(A;T)
Make rs61755794(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position42721817
GenePRPH2
is asnp
is mentioned by
dbSNPrs61755794
ebirs61755794
HLIrs61755794
Exacrs61755794
Varsomers61755794
Maprs61755794
PheGenIrs61755794
hapmaprs61755794
1000 genomesrs61755794
hgdprs61755794
ensemblrs61755794
gopubmedrs61755794
geneviewrs61755794
scholarrs61755794
googlers61755794
pharmgkbrs61755794
gwascentralrs61755794
openSNPrs61755794
23andMers61755794
23andMe allrs61755794
SNP Nexus

SNPshotrs61755794
SNPdbers61755794
MSV3drs61755794
GWAS Ctlgrs61755794
Max Magnitude0
OMIM179605
Desc
Variant0020
Relatedalso


ClinVar
Risk rs61755794(T;T)
Alt rs61755794(T;T)
Reference rs61755794(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 7 not provided
Variation info
Gene PRPH2
CLNDBN Retinitis pigmentosa 7 not provided
Reversed 1
HGVS NC_000006.11:g.42689555T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014069.18, RCV000084983.1,