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rs72558407

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558407(C;C)
Make rs72558407(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403679
GeneOTC
is asnp
is mentioned by
dbSNPrs72558407
ebirs72558407
HLIrs72558407
Exacrs72558407
Varsomers72558407
Maprs72558407
PheGenIrs72558407
hapmaprs72558407
1000 genomesrs72558407
hgdprs72558407
ensemblrs72558407
gopubmedrs72558407
geneviewrs72558407
scholarrs72558407
googlers72558407
pharmgkbrs72558407
gwascentralrs72558407
openSNPrs72558407
23andMers72558407
23andMe allrs72558407
SNP Nexus

SNPshotrs72558407
SNPdbers72558407
MSV3drs72558407
GWAS Ctlgrs72558407
Max Magnitude0
ClinVar
Risk rs72558407(C;C)
Alt rs72558407(C;C)
Reference rs72558407(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262932T>C
CLNSRC ClinVar
CLNACC RCV000083508.1,