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rs62638651

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs62638651(C;T)
Make rs62638651(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38310690
GeneRPGR
is asnp
is mentioned by
dbSNPrs62638651
ebirs62638651
HLIrs62638651
Exacrs62638651
Varsomers62638651
Maprs62638651
PheGenIrs62638651
hapmaprs62638651
1000 genomesrs62638651
hgdprs62638651
ensemblrs62638651
gopubmedrs62638651
geneviewrs62638651
scholarrs62638651
googlers62638651
pharmgkbrs62638651
gwascentralrs62638651
openSNPrs62638651
23andMers62638651
23andMe allrs62638651
SNP Nexus

SNPshotrs62638651
SNPdbers62638651
MSV3drs62638651
GWAS Ctlgrs62638651
Max Magnitude0
OMIM312610
Desc
Variant0002
Relatedalso


ClinVar
Risk rs62638651(T;T)
Alt rs62638651(T;T)
Reference rs62638651(C;C)
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.38169943G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010576.4, RCV000085116.1,