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rs72556274

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556274(C;G)
Make rs72556274(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401379
GeneOTC
is asnp
is mentioned by
dbSNPrs72556274
ebirs72556274
HLIrs72556274
Exacrs72556274
Varsomers72556274
Maprs72556274
PheGenIrs72556274
hapmaprs72556274
1000 genomesrs72556274
hgdprs72556274
ensemblrs72556274
gopubmedrs72556274
geneviewrs72556274
scholarrs72556274
googlers72556274
pharmgkbrs72556274
gwascentralrs72556274
openSNPrs72556274
23andMers72556274
23andMe allrs72556274
SNP Nexus

SNPshotrs72556274
SNPdbers72556274
MSV3drs72556274
GWAS Ctlgrs72556274
Max Magnitude0
ClinVar
Risk rs72556274(G;G)
Alt rs72556274(G;G)
Reference rs72556274(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260632C>G
CLNSRC ClinVar
CLNACC RCV000083460.1,