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rs72554326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72554326(C;T)
Make rs72554326(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367418
GeneOTC
is asnp
is mentioned by
dbSNPrs72554326
ebirs72554326
HLIrs72554326
Exacrs72554326
Varsomers72554326
Maprs72554326
PheGenIrs72554326
hapmaprs72554326
1000 genomesrs72554326
hgdprs72554326
ensemblrs72554326
gopubmedrs72554326
geneviewrs72554326
scholarrs72554326
googlers72554326
pharmgkbrs72554326
gwascentralrs72554326
openSNPrs72554326
23andMers72554326
23andMe allrs72554326
SNP Nexus

SNPshotrs72554326
SNPdbers72554326
MSV3drs72554326
GWAS Ctlgrs72554326
Max Magnitude0
ClinVar
Risk rs72554326(T;T)
Alt rs72554326(T;T)
Reference rs72554326(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226671C>T
CLNSRC ClinVar
CLNACC RCV000083362.1,