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rs878853326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853326(C;T)
Make rs878853326(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position54626631
GeneRP1
is asnp
is mentioned by
dbSNPrs878853326
ClinGenrs878853326
ebirs878853326
HLIrs878853326
Exacrs878853326
Varsomers878853326
Maprs878853326
PheGenIrs878853326
hapmaprs878853326
1000 genomesrs878853326
hgdprs878853326
ensemblrs878853326
gopubmedrs878853326
geneviewrs878853326
scholarrs878853326
googlers878853326
pharmgkbrs878853326
gwascentralrs878853326
openSNPrs878853326
23andMers878853326
23andMe allrs878853326
SNP Nexus

SNPshotrs878853326
SNPdbers878853326
MSV3drs878853326
GWAS Ctlgrs878853326
Max Magnitude0
ClinVar
Risk rs878853326(T;T)
Alt rs878853326(T;T)
Reference Rs878853326(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene RP1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000008.10:g.55539191C>T
CLNSRC
CLNACC RCV000225583.1,