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rs878853327

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853327(-;-)
Make rs878853327(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position54625344
GeneRP1
is asnp
is mentioned by
dbSNPrs878853327
ebirs878853327
HLIrs878853327
Exacrs878853327
Varsomers878853327
Maprs878853327
PheGenIrs878853327
hapmaprs878853327
1000 genomesrs878853327
hgdprs878853327
ensemblrs878853327
gopubmedrs878853327
geneviewrs878853327
scholarrs878853327
googlers878853327
pharmgkbrs878853327
gwascentralrs878853327
openSNPrs878853327
23andMers878853327
23andMe allrs878853327
SNP Nexus

SNPshotrs878853327
SNPdbers878853327
MSV3drs878853327
GWAS Ctlgrs878853327
Max Magnitude0
ClinVar
Risk rs878853327(;)
Alt rs878853327(;)
Reference rs878853327(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene RP1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000008.10:g.55537904delG
CLNSRC
CLNACC RCV000225399.1,