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rs72554316

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72554316(A;C)
Make rs72554316(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367358
GeneOTC
is asnp
is mentioned by
dbSNPrs72554316
ebirs72554316
HLIrs72554316
Exacrs72554316
Varsomers72554316
Maprs72554316
PheGenIrs72554316
hapmaprs72554316
1000 genomesrs72554316
hgdprs72554316
ensemblrs72554316
gopubmedrs72554316
geneviewrs72554316
scholarrs72554316
googlers72554316
pharmgkbrs72554316
gwascentralrs72554316
openSNPrs72554316
23andMers72554316
23andMe allrs72554316
SNP Nexus

SNPshotrs72554316
SNPdbers72554316
MSV3drs72554316
GWAS Ctlgrs72554316
Max Magnitude0
ClinVar
Risk rs72554316(C;C)
Alt rs72554316(C;C)
Reference rs72554316(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226611A>C
CLNSRC ClinVar
CLNACC RCV000083344.1,