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rs72554310

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72554310(C;T)
Make rs72554310(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367344
GeneOTC
is asnp
is mentioned by
dbSNPrs72554310
ebirs72554310
HLIrs72554310
Exacrs72554310
Varsomers72554310
Maprs72554310
PheGenIrs72554310
hapmaprs72554310
1000 genomesrs72554310
hgdprs72554310
ensemblrs72554310
gopubmedrs72554310
geneviewrs72554310
scholarrs72554310
googlers72554310
pharmgkbrs72554310
gwascentralrs72554310
openSNPrs72554310
23andMers72554310
23andMe allrs72554310
SNP Nexus

SNPshotrs72554310
SNPdbers72554310
MSV3drs72554310
GWAS Ctlgrs72554310
Max Magnitude0
ClinVar
Risk rs72554310(T;T)
Alt rs72554310(T;T)
Reference rs72554310(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226597C>T
CLNSRC ClinVar
CLNACC RCV000083336.1,