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rs72558405

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558405(A;G)
Make rs72558405(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403672
GeneOTC
is asnp
is mentioned by
dbSNPrs72558405
ebirs72558405
HLIrs72558405
Exacrs72558405
Varsomers72558405
Maprs72558405
PheGenIrs72558405
hapmaprs72558405
1000 genomesrs72558405
hgdprs72558405
ensemblrs72558405
gopubmedrs72558405
geneviewrs72558405
scholarrs72558405
googlers72558405
pharmgkbrs72558405
gwascentralrs72558405
openSNPrs72558405
23andMers72558405
23andMe allrs72558405
SNP Nexus

SNPshotrs72558405
SNPdbers72558405
MSV3drs72558405
GWAS Ctlgrs72558405
Max Magnitude0
ClinVar
Risk rs72558405(G;G)
Alt rs72558405(G;G)
Reference rs72558405(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262925A>G
CLNSRC ClinVar
CLNACC RCV000083506.1,