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rs72556280

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556280(C;G)
Make rs72556280(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401404
GeneOTC
is asnp
is mentioned by
dbSNPrs72556280
ebirs72556280
HLIrs72556280
Exacrs72556280
Varsomers72556280
Maprs72556280
PheGenIrs72556280
hapmaprs72556280
1000 genomesrs72556280
hgdprs72556280
ensemblrs72556280
gopubmedrs72556280
geneviewrs72556280
scholarrs72556280
googlers72556280
pharmgkbrs72556280
gwascentralrs72556280
openSNPrs72556280
23andMers72556280
23andMe allrs72556280
SNP Nexus

SNPshotrs72556280
SNPdbers72556280
MSV3drs72556280
GWAS Ctlgrs72556280
Max Magnitude0
ClinVar
Risk rs72556280(G;G)
Alt rs72556280(G;G)
Reference rs72556280(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260657C>G
CLNSRC ClinVar
CLNACC RCV000083470.1,