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

rs61755771

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61755771(C;T)
Make rs61755771(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position42722199
GenePRPH2
is asnp
is mentioned by
dbSNPrs61755771
ebirs61755771
HLIrs61755771
Exacrs61755771
Varsomers61755771
Maprs61755771
PheGenIrs61755771
hapmaprs61755771
1000 genomesrs61755771
hgdprs61755771
ensemblrs61755771
gopubmedrs61755771
geneviewrs61755771
scholarrs61755771
googlers61755771
pharmgkbrs61755771
gwascentralrs61755771
openSNPrs61755771
23andMers61755771
23andMe allrs61755771
SNP Nexus

SNPshotrs61755771
SNPdbers61755771
MSV3drs61755771
GWAS Ctlgrs61755771
Max Magnitude0
OMIM179605
Desc
Variant0018
Relatedalso


ClinVar
Risk rs61755771(T;T)
Alt rs61755771(T;T)
Reference rs61755771(C;C)
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.42689937G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014067.25, RCV000084955.1,