Have questions? Visit https://www.reddit.com/r/SNPedia

rs369037463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369037463(C;T)
Make rs369037463(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38317430
GeneRPGR
is asnp
is mentioned by
dbSNPrs369037463
ebirs369037463
HLIrs369037463
Exacrs369037463
Varsomers369037463
Maprs369037463
PheGenIrs369037463
hapmaprs369037463
1000 genomesrs369037463
hgdprs369037463
ensemblrs369037463
gopubmedrs369037463
geneviewrs369037463
scholarrs369037463
googlers369037463
pharmgkbrs369037463
gwascentralrs369037463
openSNPrs369037463
23andMers369037463
23andMe allrs369037463
SNP Nexus

SNPshotrs369037463
SNPdbers369037463
MSV3drs369037463
GWAS Ctlgrs369037463
Max Magnitude0
ClinVar
Risk rs369037463(A,T;A,T)
Alt rs369037463(A,T;A,T)
Reference rs369037463(C;C)
Significance Pathogenic
Disease not provided Retinitis pigmentosa 15
Variation info
Gene RPGR
CLNDBN not provided Retinitis pigmentosa 15
Reversed 0
HGVS NC_000023.10:g.38176683C>A
CLNSRC ClinVar Emory University
CLNACC RCV000078653.3, RCV000179289.1,