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rs62638634

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62638634(G;T)
Make rs62638634(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38322921
GeneRPGR
is asnp
is mentioned by
dbSNPrs62638634
ebirs62638634
HLIrs62638634
Exacrs62638634
Varsomers62638634
Maprs62638634
PheGenIrs62638634
hapmaprs62638634
1000 genomesrs62638634
hgdprs62638634
ensemblrs62638634
gopubmedrs62638634
geneviewrs62638634
scholarrs62638634
googlers62638634
pharmgkbrs62638634
gwascentralrs62638634
openSNPrs62638634
23andMers62638634
23andMe allrs62638634
SNP Nexus

SNPshotrs62638634
SNPdbers62638634
MSV3drs62638634
GWAS Ctlgrs62638634
Max Magnitude0
OMIM312610
Desc
Variant0006
Relatedalso


ClinVar
Risk rs62638634(T;T)
Alt rs62638634(T;T)
Reference rs62638634(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 15 not provided
Variation info
Gene RPGR
CLNDBN Retinitis pigmentosa 15 not provided
Reversed 1
HGVS NC_000023.10:g.38182174C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010580.4, RCV000085072.1,