Have questions? Visit https://www.reddit.com/r/SNPedia

rs72558446

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558446(G;T)
Make rs72558446(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408952
GeneOTC
is asnp
is mentioned by
dbSNPrs72558446
ebirs72558446
HLIrs72558446
Exacrs72558446
Varsomers72558446
Maprs72558446
PheGenIrs72558446
hapmaprs72558446
1000 genomesrs72558446
hgdprs72558446
ensemblrs72558446
gopubmedrs72558446
geneviewrs72558446
scholarrs72558446
googlers72558446
pharmgkbrs72558446
gwascentralrs72558446
openSNPrs72558446
23andMers72558446
23andMe allrs72558446
SNP Nexus

SNPshotrs72558446
SNPdbers72558446
MSV3drs72558446
GWAS Ctlgrs72558446
Max Magnitude0
ClinVar
Risk rs72558446(T;T)
Alt rs72558446(T;T)
Reference rs72558446(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268205G>T
CLNSRC ClinVar
CLNACC RCV000083577.1,