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rs72554350

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72554350(A;A)
Make rs72554350(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381348
GeneOTC
is asnp
is mentioned by
dbSNPrs72554350
ebirs72554350
HLIrs72554350
Exacrs72554350
Varsomers72554350
Maprs72554350
PheGenIrs72554350
hapmaprs72554350
1000 genomesrs72554350
hgdprs72554350
ensemblrs72554350
gopubmedrs72554350
geneviewrs72554350
scholarrs72554350
googlers72554350
pharmgkbrs72554350
gwascentralrs72554350
openSNPrs72554350
23andMers72554350
23andMe allrs72554350
SNP Nexus

SNPshotrs72554350
SNPdbers72554350
MSV3drs72554350
GWAS Ctlgrs72554350
Max Magnitude0
ClinVar
Risk rs72554350(A;A)
Alt rs72554350(A;A)
Reference rs72554350(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240601C>A
CLNSRC ClinVar
CLNACC RCV000083398.1,