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rs61752909

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61752909(C;C)
Make rs61752909(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position68438293
GeneRPE65
is asnp
is mentioned by
dbSNPrs61752909
ebirs61752909
HLIrs61752909
Exacrs61752909
Varsomers61752909
Maprs61752909
PheGenIrs61752909
hapmaprs61752909
1000 genomesrs61752909
hgdprs61752909
ensemblrs61752909
gopubmedrs61752909
geneviewrs61752909
scholarrs61752909
googlers61752909
pharmgkbrs61752909
gwascentralrs61752909
openSNPrs61752909
23andMers61752909
23andMe allrs61752909
SNP Nexus

SNPshotrs61752909
SNPdbers61752909
MSV3drs61752909
GWAS Ctlgrs61752909
Max Magnitude0
ClinVar
Risk rs61752909(C;C)
Alt rs61752909(C;C)
Reference rs61752909(T;T)
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.68903976A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013997.24, RCV000085141.1,