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rs72558436

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558436(A;A)
Make rs72558436(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408889
GeneOTC
is asnp
is mentioned by
dbSNPrs72558436
ebirs72558436
HLIrs72558436
Exacrs72558436
Varsomers72558436
Maprs72558436
PheGenIrs72558436
hapmaprs72558436
1000 genomesrs72558436
hgdprs72558436
ensemblrs72558436
gopubmedrs72558436
geneviewrs72558436
scholarrs72558436
googlers72558436
pharmgkbrs72558436
gwascentralrs72558436
openSNPrs72558436
23andMers72558436
23andMe allrs72558436
SNP Nexus

SNPshotrs72558436
SNPdbers72558436
MSV3drs72558436
GWAS Ctlgrs72558436
Max Magnitude0
ClinVar
Risk rs72558436(A;A)
Alt rs72558436(A;A)
Reference rs72558436(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268142T>A
CLNSRC ClinVar
CLNACC RCV000083552.1,