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rs72556281

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556281(C;C)
Make rs72556281(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401408
GeneOTC
is asnp
is mentioned by
dbSNPrs72556281
ebirs72556281
HLIrs72556281
Exacrs72556281
Varsomers72556281
Maprs72556281
PheGenIrs72556281
hapmaprs72556281
1000 genomesrs72556281
hgdprs72556281
ensemblrs72556281
gopubmedrs72556281
geneviewrs72556281
scholarrs72556281
googlers72556281
pharmgkbrs72556281
gwascentralrs72556281
openSNPrs72556281
23andMers72556281
23andMe allrs72556281
SNP Nexus

SNPshotrs72556281
SNPdbers72556281
MSV3drs72556281
GWAS Ctlgrs72556281
Max Magnitude0
ClinVar
Risk rs72556281(C;C)
Alt rs72556281(C;C)
Reference rs72556281(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260661G>C
CLNSRC ClinVar
CLNACC RCV000083471.1,