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rs72558489

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558489(C;C)
Make rs72558489(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421035
GeneOTC
is asnp
is mentioned by
dbSNPrs72558489
ebirs72558489
HLIrs72558489
Exacrs72558489
Varsomers72558489
Maprs72558489
PheGenIrs72558489
hapmaprs72558489
1000 genomesrs72558489
hgdprs72558489
ensemblrs72558489
gopubmedrs72558489
geneviewrs72558489
scholarrs72558489
googlers72558489
pharmgkbrs72558489
gwascentralrs72558489
openSNPrs72558489
23andMers72558489
23andMe allrs72558489
SNP Nexus

SNPshotrs72558489
SNPdbers72558489
MSV3drs72558489
GWAS Ctlgrs72558489
Max Magnitude0
ClinVar
Risk rs72558489(C;C)
Alt rs72558489(C;C)
Reference rs72558489(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280288T>C
CLNSRC ClinVar
CLNACC RCV000083321.1,