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rs527236112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236112(C;C)
Make rs527236112(C;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position38304647
GeneRPGR
is asnp
is mentioned by
dbSNPrs527236112
ebirs527236112
HLIrs527236112
Exacrs527236112
Varsomers527236112
Maprs527236112
PheGenIrs527236112
hapmaprs527236112
1000 genomesrs527236112
hgdprs527236112
ensemblrs527236112
gopubmedrs527236112
geneviewrs527236112
scholarrs527236112
googlers527236112
pharmgkbrs527236112
gwascentralrs527236112
openSNPrs527236112
23andMers527236112
23andMe allrs527236112
SNP Nexus

SNPshotrs527236112
SNPdbers527236112
MSV3drs527236112
GWAS Ctlgrs527236112
Max Magnitude0
ClinVar
Risk rs527236112(C;C)
Alt rs527236112(C;C)
Reference rs527236112(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RPGR
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000023.10:g.38163900C>G
CLNSRC ClinVar
CLNACC RCV000132614.1,