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rs72558451

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558451(C;T)
Make rs72558451(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408966
GeneOTC
is asnp
is mentioned by
dbSNPrs72558451
ebirs72558451
HLIrs72558451
Exacrs72558451
Varsomers72558451
Maprs72558451
PheGenIrs72558451
hapmaprs72558451
1000 genomesrs72558451
hgdprs72558451
ensemblrs72558451
gopubmedrs72558451
geneviewrs72558451
scholarrs72558451
googlers72558451
pharmgkbrs72558451
gwascentralrs72558451
openSNPrs72558451
23andMers72558451
23andMe allrs72558451
SNP Nexus

SNPshotrs72558451
SNPdbers72558451
MSV3drs72558451
GWAS Ctlgrs72558451
Max Magnitude0
ClinVar
Risk rs72558451(G,T;G,T)
Alt rs72558451(G,T;G,T)
Reference rs72558451(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268219C>G; NC_000023.10:g.38268219C>T
CLNSRC ClinVar Emory University
CLNACC RCV000079088.4, RCV000083582.1,