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rs72558452

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
(I;I) 0
Make rs72558452(-;-)
Make rs72558452(-;GAG)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408975
GeneOTC
is asnp
is mentioned by
dbSNPrs72558452
ebirs72558452
HLIrs72558452
Exacrs72558452
Varsomers72558452
Maprs72558452
PheGenIrs72558452
hapmaprs72558452
1000 genomesrs72558452
hgdprs72558452
ensemblrs72558452
gopubmedrs72558452
geneviewrs72558452
scholarrs72558452
googlers72558452
pharmgkbrs72558452
gwascentralrs72558452
openSNPrs72558452
23andMers72558452
23andMe allrs72558452
SNP Nexus

SNPshotrs72558452
SNPdbers72558452
MSV3drs72558452
GWAS Ctlgrs72558452
Max Magnitude0
ClinVar
Risk rs72558452(;)
Alt rs72558452(;)
Reference rs72558452(GAG;GAG)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268228_38268230delGAG
CLNSRC ClinVar
CLNACC RCV000083584.1,