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rs72558427

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558427(C;C)
Make rs72558427(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403742
GeneOTC
is asnp
is mentioned by
dbSNPrs72558427
ebirs72558427
HLIrs72558427
Exacrs72558427
Varsomers72558427
Maprs72558427
PheGenIrs72558427
hapmaprs72558427
1000 genomesrs72558427
hgdprs72558427
ensemblrs72558427
gopubmedrs72558427
geneviewrs72558427
scholarrs72558427
googlers72558427
pharmgkbrs72558427
gwascentralrs72558427
openSNPrs72558427
23andMers72558427
23andMe allrs72558427
SNP Nexus

SNPshotrs72558427
SNPdbers72558427
MSV3drs72558427
GWAS Ctlgrs72558427
Max Magnitude0
ClinVar
Risk rs72558427(C;C)
Alt rs72558427(C;C)
Reference rs72558427(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262995T>C
CLNSRC ClinVar
CLNACC RCV000083529.1,