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rs62638644

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs62638644(G;G)
Make rs62638644(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38318909
GeneRPGR
is asnp
is mentioned by
dbSNPrs62638644
ebirs62638644
HLIrs62638644
Exacrs62638644
Varsomers62638644
Maprs62638644
PheGenIrs62638644
hapmaprs62638644
1000 genomesrs62638644
hgdprs62638644
ensemblrs62638644
gopubmedrs62638644
geneviewrs62638644
scholarrs62638644
googlers62638644
pharmgkbrs62638644
gwascentralrs62638644
openSNPrs62638644
23andMers62638644
23andMe allrs62638644
SNP Nexus

SNPshotrs62638644
SNPdbers62638644
MSV3drs62638644
GWAS Ctlgrs62638644
Max Magnitude0
OMIM312610
Desc
Variant0001
Relatedalso


ClinVar
Risk rs62638644(G;G)
Alt rs62638644(G;G)
Reference rs62638644(T;T)
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.38178162A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010575.2, RCV000085105.1,