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rs72552296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72552296(A;A)
Make rs72552296(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38352699
GeneOTC
is asnp
is mentioned by
dbSNPrs72552296
ebirs72552296
HLIrs72552296
Exacrs72552296
Varsomers72552296
Maprs72552296
PheGenIrs72552296
hapmaprs72552296
1000 genomesrs72552296
hgdprs72552296
ensemblrs72552296
gopubmedrs72552296
geneviewrs72552296
scholarrs72552296
googlers72552296
pharmgkbrs72552296
gwascentralrs72552296
openSNPrs72552296
23andMers72552296
23andMe allrs72552296
SNP Nexus

SNPshotrs72552296
SNPdbers72552296
MSV3drs72552296
GWAS Ctlgrs72552296
Max Magnitude0
ClinVar
Risk rs72552296(A;A)
Alt rs72552296(A;A)
Reference rs72552296(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38211952G>A
CLNSRC ClinVar
CLNACC RCV000083424.1,