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rs72558475

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558475(A;A)
Make rs72558475(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411956
GeneOTC
is asnp
is mentioned by
dbSNPrs72558475
dbSNP (old)rs72558475
ClinGenrs72558475
ebirs72558475
HLIrs72558475
Exacrs72558475
Gnomadrs72558475
Varsomers72558475
Maprs72558475
PheGenIrs72558475
Biobankrs72558475
1000 genomesrs72558475
hgdprs72558475
ensemblrs72558475
gopubmedrs72558475
geneviewrs72558475
scholarrs72558475
googlers72558475
pharmgkbrs72558475
gwascentralrs72558475
openSNPrs72558475
23andMers72558475
23andMe allrs72558475
SNP Nexus

SNPshotrs72558475
SNPdbers72558475
MSV3drs72558475
GWAS Ctlgrs72558475
Max Magnitude0
ClinVar
Risk rs72558475(A;A)
Alt rs72558475(A;A)
Reference Rs72558475(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271209C>A
CLNSRC ClinVar
CLNACC RCV000083622.1,