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rs878853334

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853334(C;T)
Make rs878853334(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
GenePRPF31
is asnp
is mentioned by
dbSNPrs878853334
ebirs878853334
HLIrs878853334
Exacrs878853334
Varsomers878853334
Maprs878853334
PheGenIrs878853334
hapmaprs878853334
1000 genomesrs878853334
hgdprs878853334
ensemblrs878853334
gopubmedrs878853334
geneviewrs878853334
scholarrs878853334
googlers878853334
pharmgkbrs878853334
gwascentralrs878853334
openSNPrs878853334
23andMers878853334
23andMe allrs878853334
SNP Nexus

SNPshotrs878853334
SNPdbers878853334
MSV3drs878853334
GWAS Ctlgrs878853334
Max Magnitude0
ClinVar
Risk rs878853334(T;T)
Alt rs878853334(T;T)
Reference rs878853334(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene PRPF31
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000019.9:g.54631496C>T
CLNSRC
CLNACC RCV000225503.1,