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rs72558490

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558490(C;C)
Make rs72558490(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421039
GeneOTC
is asnp
is mentioned by
dbSNPrs72558490
ebirs72558490
HLIrs72558490
Exacrs72558490
Varsomers72558490
Maprs72558490
PheGenIrs72558490
hapmaprs72558490
1000 genomesrs72558490
hgdprs72558490
ensemblrs72558490
gopubmedrs72558490
geneviewrs72558490
scholarrs72558490
googlers72558490
pharmgkbrs72558490
gwascentralrs72558490
openSNPrs72558490
23andMers72558490
23andMe allrs72558490
SNP Nexus

SNPshotrs72558490
SNPdbers72558490
MSV3drs72558490
GWAS Ctlgrs72558490
Max Magnitude0
ClinVar
Risk rs72558490(C;C)
Alt rs72558490(C;C)
Reference rs72558490(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280292T>C
CLNSRC ClinVar
CLNACC RCV000083322.1,