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rs61752871

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61752871(C;T)
Make rs61752871(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position68444858
GeneRPE65
is asnp
is mentioned by
dbSNPrs61752871
ebirs61752871
HLIrs61752871
Exacrs61752871
Varsomers61752871
Maprs61752871
PheGenIrs61752871
hapmaprs61752871
1000 genomesrs61752871
hgdprs61752871
ensemblrs61752871
gopubmedrs61752871
geneviewrs61752871
scholarrs61752871
googlers61752871
pharmgkbrs61752871
gwascentralrs61752871
openSNPrs61752871
23andMers61752871
23andMe allrs61752871
SNP Nexus

SNPshotrs61752871
SNPdbers61752871
MSV3drs61752871
GWAS Ctlgrs61752871
Max Magnitude0
ClinVar
Risk rs61752871(T;T)
Alt rs61752871(T;T)
Reference rs61752871(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 20 not provided
Variation info
Gene RPE65
CLNDBN Retinitis pigmentosa 20 not provided
Reversed 1
HGVS NC_000001.10:g.68910541G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013994.17, RCV000085184.1,