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rs398122960

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs398122960(-;-)
Make rs398122960(-;AG)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38286593
GeneRPGR
is asnp
is mentioned by
dbSNPrs398122960
ebirs398122960
HLIrs398122960
Exacrs398122960
Varsomers398122960
Maprs398122960
PheGenIrs398122960
hapmaprs398122960
1000 genomesrs398122960
hgdprs398122960
ensemblrs398122960
gopubmedrs398122960
geneviewrs398122960
scholarrs398122960
googlers398122960
pharmgkbrs398122960
gwascentralrs398122960
openSNPrs398122960
23andMers398122960
23andMe allrs398122960
SNP Nexus

SNPshotrs398122960
SNPdbers398122960
MSV3drs398122960
GWAS Ctlgrs398122960
Max Magnitude0
ClinVar
Risk rs398122960(;)
Alt rs398122960(;)
Reference rs398122960(AG;AG)
Significance Pathogenic
Disease Retinitis pigmentosa 15
Variation info
Gene RPGR
CLNDBN Retinitis pigmentosa 15
Reversed 1
HGVS NC_000023.10:g.38145846_38145847delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000076907.3,