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rs527236094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236094(G;T)
Make rs527236094(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
GeneAC012314.8, PRPF31
is asnp
is mentioned by
dbSNPrs527236094
ebirs527236094
HLIrs527236094
Exacrs527236094
Varsomers527236094
Maprs527236094
PheGenIrs527236094
hapmaprs527236094
1000 genomesrs527236094
hgdprs527236094
ensemblrs527236094
gopubmedrs527236094
geneviewrs527236094
scholarrs527236094
googlers527236094
pharmgkbrs527236094
gwascentralrs527236094
openSNPrs527236094
23andMers527236094
23andMe allrs527236094
SNP Nexus

SNPshotrs527236094
SNPdbers527236094
MSV3drs527236094
GWAS Ctlgrs527236094
Max Magnitude0
ClinVar
Risk rs527236094(T;T)
Alt rs527236094(T;T)
Reference rs527236094(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene PRPF31 LOC101928780
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000019.9:g.54627162G>T
CLNSRC ClinVar
CLNACC RCV000132673.1,