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rs72554318

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72554318(A;T)
Make rs72554318(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367369
GeneOTC
is asnp
is mentioned by
dbSNPrs72554318
ebirs72554318
HLIrs72554318
Exacrs72554318
Varsomers72554318
Maprs72554318
PheGenIrs72554318
hapmaprs72554318
1000 genomesrs72554318
hgdprs72554318
ensemblrs72554318
gopubmedrs72554318
geneviewrs72554318
scholarrs72554318
googlers72554318
pharmgkbrs72554318
gwascentralrs72554318
openSNPrs72554318
23andMers72554318
23andMe allrs72554318
SNP Nexus

SNPshotrs72554318
SNPdbers72554318
MSV3drs72554318
GWAS Ctlgrs72554318
Max Magnitude0
ClinVar
Risk rs72554318(T;T)
Alt rs72554318(T;T)
Reference rs72554318(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226622A>T
CLNSRC ClinVar
CLNACC RCV000083350.1,