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rs527236079

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236079(C;T)
Make rs527236079(T;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position154744489
GeneLRAT
is asnp
is mentioned by
dbSNPrs527236079
ebirs527236079
HLIrs527236079
Exacrs527236079
Varsomers527236079
Maprs527236079
PheGenIrs527236079
hapmaprs527236079
1000 genomesrs527236079
hgdprs527236079
ensemblrs527236079
gopubmedrs527236079
geneviewrs527236079
scholarrs527236079
googlers527236079
pharmgkbrs527236079
gwascentralrs527236079
openSNPrs527236079
23andMers527236079
23andMe allrs527236079
SNP Nexus

SNPshotrs527236079
SNPdbers527236079
MSV3drs527236079
GWAS Ctlgrs527236079
Max Magnitude0
ClinVar
Risk rs527236079(T;T)
Alt rs527236079(T;T)
Reference rs527236079(C;C)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene LRAT
CLNDBN Retinitis pigmentosa
Reversed 0
HGVS NC_000004.11:g.155665641C>T
CLNSRC ClinVar
CLNACC RCV000132653.1,