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rs878853335

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853335(G;T)
Make rs878853335(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
GenePRPF31
is asnp
is mentioned by
dbSNPrs878853335
ebirs878853335
HLIrs878853335
Exacrs878853335
Varsomers878853335
Maprs878853335
PheGenIrs878853335
hapmaprs878853335
1000 genomesrs878853335
hgdprs878853335
ensemblrs878853335
gopubmedrs878853335
geneviewrs878853335
scholarrs878853335
googlers878853335
pharmgkbrs878853335
gwascentralrs878853335
openSNPrs878853335
23andMers878853335
23andMe allrs878853335
SNP Nexus

SNPshotrs878853335
SNPdbers878853335
MSV3drs878853335
GWAS Ctlgrs878853335
Max Magnitude0
ClinVar
Risk rs878853335(T;T)
Alt rs878853335(T;T)
Reference rs878853335(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene PRPF31
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000019.9:g.54631469G>T
CLNSRC
CLNACC RCV000225424.1,