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rs72554346

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554346(C;C)
Make rs72554346(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369863
GeneOTC
is asnp
is mentioned by
dbSNPrs72554346
ebirs72554346
HLIrs72554346
Exacrs72554346
Varsomers72554346
Maprs72554346
PheGenIrs72554346
hapmaprs72554346
1000 genomesrs72554346
hgdprs72554346
ensemblrs72554346
gopubmedrs72554346
geneviewrs72554346
scholarrs72554346
googlers72554346
pharmgkbrs72554346
gwascentralrs72554346
openSNPrs72554346
23andMers72554346
23andMe allrs72554346
SNP Nexus

SNPshotrs72554346
SNPdbers72554346
MSV3drs72554346
GWAS Ctlgrs72554346
Max Magnitude0
ClinVar
Risk rs72554346(C;C)
Alt rs72554346(C;C)
Reference rs72554346(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229116T>C
CLNSRC ClinVar
CLNACC RCV000083389.1,