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rs62642057

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs62642057(A;A)
Make rs62642057(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38304746
GeneRPGR
is asnp
is mentioned by
dbSNPrs62642057
ebirs62642057
HLIrs62642057
Exacrs62642057
Varsomers62642057
Maprs62642057
PheGenIrs62642057
hapmaprs62642057
1000 genomesrs62642057
hgdprs62642057
ensemblrs62642057
gopubmedrs62642057
geneviewrs62642057
scholarrs62642057
googlers62642057
pharmgkbrs62642057
gwascentralrs62642057
openSNPrs62642057
23andMers62642057
23andMe allrs62642057
SNP Nexus

SNPshotrs62642057
SNPdbers62642057
MSV3drs62642057
GWAS Ctlgrs62642057
Max Magnitude0
OMIM312610
Desc
Variant0003
Relatedalso


ClinVar
Risk rs62642057(A;A)
Alt rs62642057(A;A)
Reference rs62642057(G;G)
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.38163999C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010577.5, RCV000085125.1,