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rs72554337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554337(A;A)
Make rs72554337(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369827
GeneOTC
is asnp
is mentioned by
dbSNPrs72554337
ebirs72554337
HLIrs72554337
Exacrs72554337
Varsomers72554337
Maprs72554337
PheGenIrs72554337
hapmaprs72554337
1000 genomesrs72554337
hgdprs72554337
ensemblrs72554337
gopubmedrs72554337
geneviewrs72554337
scholarrs72554337
googlers72554337
pharmgkbrs72554337
gwascentralrs72554337
openSNPrs72554337
23andMers72554337
23andMe allrs72554337
SNP Nexus

SNPshotrs72554337
SNPdbers72554337
MSV3drs72554337
GWAS Ctlgrs72554337
Max Magnitude0
ClinVar
Risk rs72554337(A;A)
Alt rs72554337(A;A)
Reference rs72554337(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229080G>A
CLNSRC ClinVar
CLNACC RCV000083375.1,