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rs72554328

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72554328(C;C)
Make rs72554328(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369806
GeneOTC
is asnp
is mentioned by
dbSNPrs72554328
ebirs72554328
HLIrs72554328
Exacrs72554328
Varsomers72554328
Maprs72554328
PheGenIrs72554328
hapmaprs72554328
1000 genomesrs72554328
hgdprs72554328
ensemblrs72554328
gopubmedrs72554328
geneviewrs72554328
scholarrs72554328
googlers72554328
pharmgkbrs72554328
gwascentralrs72554328
openSNPrs72554328
23andMers72554328
23andMe allrs72554328
SNP Nexus

SNPshotrs72554328
SNPdbers72554328
MSV3drs72554328
GWAS Ctlgrs72554328
Max Magnitude0
ClinVar
Risk rs72554328(C;C)
Alt rs72554328(C;C)
Reference rs72554328(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229059T>C
CLNSRC ClinVar
CLNACC RCV000083366.1,