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

rs62638646

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62638646(A;A)
Make rs62638646(A;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position38318828
GeneRPGR
is asnp
is mentioned by
dbSNPrs62638646
ebirs62638646
HLIrs62638646
Exacrs62638646
Varsomers62638646
Maprs62638646
PheGenIrs62638646
hapmaprs62638646
1000 genomesrs62638646
hgdprs62638646
ensemblrs62638646
gopubmedrs62638646
geneviewrs62638646
scholarrs62638646
googlers62638646
pharmgkbrs62638646
gwascentralrs62638646
openSNPrs62638646
23andMers62638646
23andMe allrs62638646
SNP Nexus

SNPshotrs62638646
SNPdbers62638646
MSV3drs62638646
GWAS Ctlgrs62638646
Max Magnitude0
ClinVar
Risk rs62638646(A;A)
Alt rs62638646(A;A)
Reference rs62638646(G;G)
Significance Probable-Pathogenic
Disease not provided Retinitis pigmentosa
Variation info
Gene RPGR
CLNDBN not provided Retinitis pigmentosa
Reversed 1
HGVS NC_000023.10:g.38178081C>T
CLNSRC ClinVar Retina International
CLNACC RCV000085107.1, RCV000132611.1,