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rs137852549

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852549(G;T)
Make rs137852549(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38286349
GeneRPGR
is asnp
is mentioned by
dbSNPrs137852549
ebirs137852549
HLIrs137852549
Exacrs137852549
Varsomers137852549
Maprs137852549
PheGenIrs137852549
hapmaprs137852549
1000 genomesrs137852549
hgdprs137852549
ensemblrs137852549
gopubmedrs137852549
geneviewrs137852549
scholarrs137852549
googlers137852549
pharmgkbrs137852549
gwascentralrs137852549
openSNPrs137852549
23andMers137852549
23andMe allrs137852549
SNP Nexus

SNPshotrs137852549
SNPdbers137852549
MSV3drs137852549
GWAS Ctlgrs137852549
Max Magnitude0
OMIM312610
Desc
Variant0012
Relatedalso
ClinVar
Risk rs137852549(T;T)
Alt rs137852549(T;T)
Reference rs137852549(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 15
Variation info
Gene RPGR
CLNDBN Retinitis pigmentosa 15
Reversed 1
HGVS NC_000023.10:g.38145602C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010586.3,