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rs72556298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556298(C;G)
Make rs72556298(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403653
GeneOTC
is asnp
is mentioned by
dbSNPrs72556298
ebirs72556298
HLIrs72556298
Exacrs72556298
Varsomers72556298
Maprs72556298
PheGenIrs72556298
hapmaprs72556298
1000 genomesrs72556298
hgdprs72556298
ensemblrs72556298
gopubmedrs72556298
geneviewrs72556298
scholarrs72556298
googlers72556298
pharmgkbrs72556298
gwascentralrs72556298
openSNPrs72556298
23andMers72556298
23andMe allrs72556298
SNP Nexus

SNPshotrs72556298
SNPdbers72556298
MSV3drs72556298
GWAS Ctlgrs72556298
Max Magnitude0
ClinVar
Risk rs72556298(G;G)
Alt rs72556298(G;G)
Reference rs72556298(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262906C>G
CLNSRC ClinVar
CLNACC RCV000083493.1,