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rs72558474

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558474(G;T)
Make rs72558474(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411953
GeneOTC
is asnp
is mentioned by
dbSNPrs72558474
ebirs72558474
HLIrs72558474
Exacrs72558474
Varsomers72558474
Maprs72558474
PheGenIrs72558474
hapmaprs72558474
1000 genomesrs72558474
hgdprs72558474
ensemblrs72558474
gopubmedrs72558474
geneviewrs72558474
scholarrs72558474
googlers72558474
pharmgkbrs72558474
gwascentralrs72558474
openSNPrs72558474
23andMers72558474
23andMe allrs72558474
SNP Nexus

SNPshotrs72558474
SNPdbers72558474
MSV3drs72558474
GWAS Ctlgrs72558474
Max Magnitude0
ClinVar
Risk rs72558474(T;T)
Alt rs72558474(T;T)
Reference rs72558474(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271206G>T
CLNSRC ClinVar
CLNACC RCV000083621.1,