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rs62638632

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs62638632(A;G)
Make rs62638632(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38322947
GeneRPGR
is asnp
is mentioned by
dbSNPrs62638632
ebirs62638632
HLIrs62638632
Exacrs62638632
Varsomers62638632
Maprs62638632
PheGenIrs62638632
hapmaprs62638632
1000 genomesrs62638632
hgdprs62638632
ensemblrs62638632
gopubmedrs62638632
geneviewrs62638632
scholarrs62638632
googlers62638632
pharmgkbrs62638632
gwascentralrs62638632
openSNPrs62638632
23andMers62638632
23andMe allrs62638632
SNP Nexus

SNPshotrs62638632
SNPdbers62638632
MSV3drs62638632
GWAS Ctlgrs62638632
Max Magnitude0
ClinVar
Risk rs62638632(G;G)
Alt rs62638632(G;G)
Reference rs62638632(A;A)
Significance Pathogenic
Disease not provided Retinitis pigmentosa 15
Variation info
Gene RPGR
CLNDBN not provided Retinitis pigmentosa 15
Reversed 1
HGVS NC_000023.10:g.38182200T>C
CLNSRC HGMD
CLNACC RCV000078647.4, RCV000177041.1,