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rs72558445

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558445(C;C)
Make rs72558445(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408951
GeneOTC
is asnp
is mentioned by
dbSNPrs72558445
ebirs72558445
HLIrs72558445
Exacrs72558445
Varsomers72558445
Maprs72558445
PheGenIrs72558445
hapmaprs72558445
1000 genomesrs72558445
hgdprs72558445
ensemblrs72558445
gopubmedrs72558445
geneviewrs72558445
scholarrs72558445
googlers72558445
pharmgkbrs72558445
gwascentralrs72558445
openSNPrs72558445
23andMers72558445
23andMe allrs72558445
SNP Nexus

SNPshotrs72558445
SNPdbers72558445
MSV3drs72558445
GWAS Ctlgrs72558445
Max Magnitude0
ClinVar
Risk rs72558445(C;C)
Alt rs72558445(C;C)
Reference rs72558445(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268204T>C
CLNSRC ClinVar
CLNACC RCV000083576.1,