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

rs72558437

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558437(A;A)
Make rs72558437(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408898
GeneOTC
is asnp
is mentioned by
dbSNPrs72558437
ebirs72558437
HLIrs72558437
Exacrs72558437
Varsomers72558437
Maprs72558437
PheGenIrs72558437
hapmaprs72558437
1000 genomesrs72558437
hgdprs72558437
ensemblrs72558437
gopubmedrs72558437
geneviewrs72558437
scholarrs72558437
googlers72558437
pharmgkbrs72558437
gwascentralrs72558437
openSNPrs72558437
23andMers72558437
23andMe allrs72558437
SNP Nexus

SNPshotrs72558437
SNPdbers72558437
MSV3drs72558437
GWAS Ctlgrs72558437
Max Magnitude0
ClinVar
Risk rs72558437(A;A)
Alt rs72558437(A;A)
Reference rs72558437(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268151C>A
CLNSRC ClinVar
CLNACC RCV000083554.2,