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rs72558482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558482(A;A)
Make rs72558482(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411990
GeneOTC
is asnp
is mentioned by
dbSNPrs72558482
ebirs72558482
HLIrs72558482
Exacrs72558482
Varsomers72558482
Maprs72558482
PheGenIrs72558482
hapmaprs72558482
1000 genomesrs72558482
hgdprs72558482
ensemblrs72558482
gopubmedrs72558482
geneviewrs72558482
scholarrs72558482
googlers72558482
pharmgkbrs72558482
gwascentralrs72558482
openSNPrs72558482
23andMers72558482
23andMe allrs72558482
SNP Nexus

SNPshotrs72558482
SNPdbers72558482
MSV3drs72558482
GWAS Ctlgrs72558482
Max Magnitude0
ClinVar
Risk rs72558482(A;A)
Alt rs72558482(A;A)
Reference rs72558482(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271243G>A
CLNSRC ClinVar
CLNACC RCV000083629.1,