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

rs398123336

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123336(A;A)
Make rs398123336(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position38304763
GeneRPGR
is asnp
is mentioned by
dbSNPrs398123336
ebirs398123336
HLIrs398123336
Exacrs398123336
Varsomers398123336
Maprs398123336
PheGenIrs398123336
hapmaprs398123336
1000 genomesrs398123336
hgdprs398123336
ensemblrs398123336
gopubmedrs398123336
geneviewrs398123336
scholarrs398123336
googlers398123336
pharmgkbrs398123336
gwascentralrs398123336
openSNPrs398123336
23andMers398123336
23andMe allrs398123336
SNP Nexus

SNPshotrs398123336
SNPdbers398123336
MSV3drs398123336
GWAS Ctlgrs398123336
Max Magnitude0
ClinVar
Risk rs398123336(A;A)
Alt rs398123336(A;A)
Reference rs398123336(G;G)
Significance Probable-Pathogenic
Disease not provided Retinitis pigmentosa 15
Variation info
Gene RPGR
CLNDBN not provided Retinitis pigmentosa 15
Reversed 1
HGVS NC_000023.10:g.38164016C>T
CLNSRC
CLNACC RCV000078654.3, RCV000180142.1,