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rs527236134

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs527236134(C;T)
Make rs527236134(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position111929428
GeneMERTK
is asnp
is mentioned by
dbSNPrs527236134
ebirs527236134
HLIrs527236134
Exacrs527236134
Varsomers527236134
Maprs527236134
PheGenIrs527236134
hapmaprs527236134
1000 genomesrs527236134
hgdprs527236134
ensemblrs527236134
gopubmedrs527236134
geneviewrs527236134
scholarrs527236134
googlers527236134
pharmgkbrs527236134
gwascentralrs527236134
openSNPrs527236134
23andMers527236134
23andMe allrs527236134
SNP Nexus

SNPshotrs527236134
SNPdbers527236134
MSV3drs527236134
GWAS Ctlgrs527236134
Max Magnitude0
ClinVar
Risk rs527236134(T;T)
Alt rs527236134(T;T)
Reference rs527236134(C;C)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa 38
Variation info
Gene MERTK
CLNDBN Retinitis pigmentosa 38
Reversed 0
HGVS NC_000002.11:g.112687005C>T
CLNSRC ClinVar
CLNACC RCV000132665.1,