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rs72558430

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558430(G;T)
Make rs72558430(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408778
GeneOTC
is asnp
is mentioned by
dbSNPrs72558430
ebirs72558430
HLIrs72558430
Exacrs72558430
Varsomers72558430
Maprs72558430
PheGenIrs72558430
hapmaprs72558430
1000 genomesrs72558430
hgdprs72558430
ensemblrs72558430
gopubmedrs72558430
geneviewrs72558430
scholarrs72558430
googlers72558430
pharmgkbrs72558430
gwascentralrs72558430
openSNPrs72558430
23andMers72558430
23andMe allrs72558430
SNP Nexus

SNPshotrs72558430
SNPdbers72558430
MSV3drs72558430
GWAS Ctlgrs72558430
Max Magnitude0
ClinVar
Risk rs72558430(T;T)
Alt rs72558430(T;T)
Reference rs72558430(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268031G>T
CLNSRC ClinVar
CLNACC RCV000083539.1,