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rs72556253

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556253(C;C)
Make rs72556253(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401282
GeneOTC
is asnp
is mentioned by
dbSNPrs72556253
ebirs72556253
HLIrs72556253
Exacrs72556253
Varsomers72556253
Maprs72556253
PheGenIrs72556253
hapmaprs72556253
1000 genomesrs72556253
hgdprs72556253
ensemblrs72556253
gopubmedrs72556253
geneviewrs72556253
scholarrs72556253
googlers72556253
pharmgkbrs72556253
gwascentralrs72556253
openSNPrs72556253
23andMers72556253
23andMe allrs72556253
SNP Nexus

SNPshotrs72556253
SNPdbers72556253
MSV3drs72556253
GWAS Ctlgrs72556253
Max Magnitude0
ClinVar
Risk rs72556253(C;C)
Alt rs72556253(C;C)
Reference rs72556253(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260535T>C
CLNSRC ClinVar
CLNACC RCV000083422.1,