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rs72556263

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556263(C;G)
Make rs72556263(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401325
GeneOTC
is asnp
is mentioned by
dbSNPrs72556263
ebirs72556263
HLIrs72556263
Exacrs72556263
Varsomers72556263
Maprs72556263
PheGenIrs72556263
hapmaprs72556263
1000 genomesrs72556263
hgdprs72556263
ensemblrs72556263
gopubmedrs72556263
geneviewrs72556263
scholarrs72556263
googlers72556263
pharmgkbrs72556263
gwascentralrs72556263
openSNPrs72556263
23andMers72556263
23andMe allrs72556263
SNP Nexus

SNPshotrs72556263
SNPdbers72556263
MSV3drs72556263
GWAS Ctlgrs72556263
Max Magnitude0
ClinVar
Risk rs72556263(G;G)
Alt rs72556263(G;G)
Reference rs72556263(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260578C>G
CLNSRC ClinVar
CLNACC RCV000083438.1,