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rs527236108

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs527236108(G;T)
Make rs527236108(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position38287018
GeneRPGR
is asnp
is mentioned by
dbSNPrs527236108
ebirs527236108
HLIrs527236108
Exacrs527236108
Varsomers527236108
Maprs527236108
PheGenIrs527236108
hapmaprs527236108
1000 genomesrs527236108
hgdprs527236108
ensemblrs527236108
gopubmedrs527236108
geneviewrs527236108
scholarrs527236108
googlers527236108
pharmgkbrs527236108
gwascentralrs527236108
openSNPrs527236108
23andMers527236108
23andMe allrs527236108
SNP Nexus

SNPshotrs527236108
SNPdbers527236108
MSV3drs527236108
GWAS Ctlgrs527236108
Max Magnitude0
ClinVar
Risk rs527236108(T;T)
Alt rs527236108(T;T)
Reference rs527236108(G;G)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RPGR
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000023.10:g.38146271C>A
CLNSRC ClinVar
CLNACC RCV000132609.1,