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rs61752878

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61752878(A;A)
Make rs61752878(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position68444632
GeneRPE65
is asnp
is mentioned by
dbSNPrs61752878
ebirs61752878
HLIrs61752878
Exacrs61752878
Varsomers61752878
Maprs61752878
PheGenIrs61752878
hapmaprs61752878
1000 genomesrs61752878
hgdprs61752878
ensemblrs61752878
gopubmedrs61752878
geneviewrs61752878
scholarrs61752878
googlers61752878
pharmgkbrs61752878
gwascentralrs61752878
openSNPrs61752878
23andMers61752878
23andMe allrs61752878
SNP Nexus

SNPshotrs61752878
SNPdbers61752878
MSV3drs61752878
GWAS Ctlgrs61752878
Max Magnitude0
ClinVar
Risk rs61752878(A;A)
Alt rs61752878(A;A)
Reference rs61752878(G;G)
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.68910315C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013998.24, RCV000085196.1,