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rs878853331

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853331(-;-)
Make rs878853331(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
GenePRPF31
is asnp
is mentioned by
dbSNPrs878853331
ebirs878853331
HLIrs878853331
Exacrs878853331
Varsomers878853331
Maprs878853331
PheGenIrs878853331
hapmaprs878853331
1000 genomesrs878853331
hgdprs878853331
ensemblrs878853331
gopubmedrs878853331
geneviewrs878853331
scholarrs878853331
googlers878853331
pharmgkbrs878853331
gwascentralrs878853331
openSNPrs878853331
23andMers878853331
23andMe allrs878853331
SNP Nexus

SNPshotrs878853331
SNPdbers878853331
MSV3drs878853331
GWAS Ctlgrs878853331
Max Magnitude0
ClinVar
Risk rs878853331(;)
Alt rs878853331(;)
Reference rs878853331(G;G)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene PRPF31
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000019.9:g.54625953delG
CLNSRC
CLNACC RCV000225511.1,