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rs730882261

From SNPedia

Orientationminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs730882261(-;-)
Make rs730882261(-;AG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position38286572
GeneRPGR
is asnp
is mentioned by
dbSNPrs730882261
ebirs730882261
HLIrs730882261
Exacrs730882261
Varsomers730882261
Maprs730882261
PheGenIrs730882261
hapmaprs730882261
1000 genomesrs730882261
hgdprs730882261
ensemblrs730882261
gopubmedrs730882261
geneviewrs730882261
scholarrs730882261
googlers730882261
pharmgkbrs730882261
gwascentralrs730882261
openSNPrs730882261
23andMers730882261
23andMe allrs730882261
SNP Nexus

SNPshotrs730882261
SNPdbers730882261
MSV3drs730882261
GWAS Ctlgrs730882261
Max Magnitude0
ClinVar
Risk rs730882261(;)
Alt rs730882261(;)
Reference rs730882261(AG;AG)
Significance Pathogenic
Disease Retinitis pigmentosa
Variation info
Gene RPGR
CLNDBN Retinitis pigmentosa
Reversed 1
HGVS NC_000023.10:g.38145825_38145826delCT
CLNSRC Inc.
CLNACC RCV000162095.1,