Have questions? Visit https://www.reddit.com/r/SNPedia

rs72554347

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554347(A;A)
Make rs72554347(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369871
GeneOTC
is asnp
is mentioned by
dbSNPrs72554347
ebirs72554347
HLIrs72554347
Exacrs72554347
Varsomers72554347
Maprs72554347
PheGenIrs72554347
hapmaprs72554347
1000 genomesrs72554347
hgdprs72554347
ensemblrs72554347
gopubmedrs72554347
geneviewrs72554347
scholarrs72554347
googlers72554347
pharmgkbrs72554347
gwascentralrs72554347
openSNPrs72554347
23andMers72554347
23andMe allrs72554347
SNP Nexus

SNPshotrs72554347
SNPdbers72554347
MSV3drs72554347
GWAS Ctlgrs72554347
Max Magnitude0
ClinVar
Risk rs72554347(A;A)
Alt rs72554347(A;A)
Reference rs72554347(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229124G>A
CLNSRC ClinVar
CLNACC RCV000083391.1,