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rs878853328

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853328(C;T)
Make rs878853328(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position54625914
GeneRP1
is asnp
is mentioned by
dbSNPrs878853328
ebirs878853328
HLIrs878853328
Exacrs878853328
Varsomers878853328
Maprs878853328
PheGenIrs878853328
hapmaprs878853328
1000 genomesrs878853328
hgdprs878853328
ensemblrs878853328
gopubmedrs878853328
geneviewrs878853328
scholarrs878853328
googlers878853328
pharmgkbrs878853328
gwascentralrs878853328
openSNPrs878853328
23andMers878853328
23andMe allrs878853328
SNP Nexus

SNPshotrs878853328
SNPdbers878853328
MSV3drs878853328
GWAS Ctlgrs878853328
Max Magnitude0
ClinVar
Risk rs878853328(T;T)
Alt rs878853328(T;T)
Reference rs878853328(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene RP1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000008.10:g.55538474C>T
CLNSRC
CLNACC RCV000225475.1,