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rs72558464

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558464(A;A)
Make rs72558464(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411902
GeneOTC
is asnp
is mentioned by
dbSNPrs72558464
ebirs72558464
HLIrs72558464
Exacrs72558464
Varsomers72558464
Maprs72558464
PheGenIrs72558464
hapmaprs72558464
1000 genomesrs72558464
hgdprs72558464
ensemblrs72558464
gopubmedrs72558464
geneviewrs72558464
scholarrs72558464
googlers72558464
pharmgkbrs72558464
gwascentralrs72558464
openSNPrs72558464
23andMers72558464
23andMe allrs72558464
SNP Nexus

SNPshotrs72558464
SNPdbers72558464
MSV3drs72558464
GWAS Ctlgrs72558464
Max Magnitude0
ClinVar
Risk rs72558464(A;A)
Alt rs72558464(A;A)
Reference rs72558464(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271155G>A
CLNSRC ClinVar
CLNACC RCV000083606.1,