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rs72556273

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556273(C;C)
Make rs72556273(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401378
GeneOTC
is asnp
is mentioned by
dbSNPrs72556273
ebirs72556273
HLIrs72556273
Exacrs72556273
Varsomers72556273
Maprs72556273
PheGenIrs72556273
hapmaprs72556273
1000 genomesrs72556273
hgdprs72556273
ensemblrs72556273
gopubmedrs72556273
geneviewrs72556273
scholarrs72556273
googlers72556273
pharmgkbrs72556273
gwascentralrs72556273
openSNPrs72556273
23andMers72556273
23andMe allrs72556273
SNP Nexus

SNPshotrs72556273
SNPdbers72556273
MSV3drs72556273
GWAS Ctlgrs72556273
Max Magnitude0
ClinVar
Risk rs72556273(C;C)
Alt rs72556273(C;C)
Reference rs72556273(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260631T>C
CLNSRC ClinVar
CLNACC RCV000083459.1,