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rs527236095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs527236095(A;T)
Make rs527236095(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
GeneAC012314.8, PRPF31
is asnp
is mentioned by
dbSNPrs527236095
ebirs527236095
HLIrs527236095
Exacrs527236095
Varsomers527236095
Maprs527236095
PheGenIrs527236095
hapmaprs527236095
1000 genomesrs527236095
hgdprs527236095
ensemblrs527236095
gopubmedrs527236095
geneviewrs527236095
scholarrs527236095
googlers527236095
pharmgkbrs527236095
gwascentralrs527236095
openSNPrs527236095
23andMers527236095
23andMe allrs527236095
SNP Nexus

SNPshotrs527236095
SNPdbers527236095
MSV3drs527236095
GWAS Ctlgrs527236095
Max Magnitude0
ClinVar
Risk rs527236095(T;T)
Alt rs527236095(T;T)
Reference rs527236095(A;A)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene PRPF31 LOC101928780
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000019.9:g.54627944A>T
CLNSRC ClinVar
CLNACC RCV000132675.1,