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

rs62638637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs62638637(A;A)
Make rs62638637(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38321041
GeneRPGR
is asnp
is mentioned by
dbSNPrs62638637
ebirs62638637
HLIrs62638637
Exacrs62638637
Varsomers62638637
Maprs62638637
PheGenIrs62638637
hapmaprs62638637
1000 genomesrs62638637
hgdprs62638637
ensemblrs62638637
gopubmedrs62638637
geneviewrs62638637
scholarrs62638637
googlers62638637
pharmgkbrs62638637
gwascentralrs62638637
openSNPrs62638637
23andMers62638637
23andMe allrs62638637
SNP Nexus

SNPshotrs62638637
SNPdbers62638637
MSV3drs62638637
GWAS Ctlgrs62638637
Max Magnitude0
OMIM312610
Desc
Variant0009
Relatedalso


ClinVar
Risk rs62638637(A;A)
Alt rs62638637(A;A)
Reference rs62638637(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.38180294G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010584.4, RCV000085096.1,