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rs72558455

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558455(C;T)
Make rs72558455(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408993
GeneOTC
is asnp
is mentioned by
dbSNPrs72558455
ebirs72558455
HLIrs72558455
Exacrs72558455
Varsomers72558455
Maprs72558455
PheGenIrs72558455
hapmaprs72558455
1000 genomesrs72558455
hgdprs72558455
ensemblrs72558455
gopubmedrs72558455
geneviewrs72558455
scholarrs72558455
googlers72558455
pharmgkbrs72558455
gwascentralrs72558455
openSNPrs72558455
23andMers72558455
23andMe allrs72558455
SNP Nexus

SNPshotrs72558455
SNPdbers72558455
MSV3drs72558455
GWAS Ctlgrs72558455
Max Magnitude0
ClinVar
Risk rs72558455(T;T)
Alt rs72558455(T;T)
Reference rs72558455(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268246C>T
CLNSRC ClinVar
CLNACC RCV000083589.1,