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rs72554359

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554359(C;C)
Make rs72554359(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381431
GeneOTC
is asnp
is mentioned by
dbSNPrs72554359
ebirs72554359
HLIrs72554359
Exacrs72554359
Varsomers72554359
Maprs72554359
PheGenIrs72554359
hapmaprs72554359
1000 genomesrs72554359
hgdprs72554359
ensemblrs72554359
gopubmedrs72554359
geneviewrs72554359
scholarrs72554359
googlers72554359
pharmgkbrs72554359
gwascentralrs72554359
openSNPrs72554359
23andMers72554359
23andMe allrs72554359
SNP Nexus

SNPshotrs72554359
SNPdbers72554359
MSV3drs72554359
GWAS Ctlgrs72554359
Max Magnitude0
ClinVar
Risk rs72554359(C;C)
Alt rs72554359(C;C)
Reference rs72554359(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240684T>C
CLNSRC ClinVar
CLNACC RCV000083413.1,