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rs72558484

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558484(C;C)
Make rs72558484(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38412001
GeneOTC
is asnp
is mentioned by
dbSNPrs72558484
ebirs72558484
HLIrs72558484
Exacrs72558484
Varsomers72558484
Maprs72558484
PheGenIrs72558484
hapmaprs72558484
1000 genomesrs72558484
hgdprs72558484
ensemblrs72558484
gopubmedrs72558484
geneviewrs72558484
scholarrs72558484
googlers72558484
pharmgkbrs72558484
gwascentralrs72558484
openSNPrs72558484
23andMers72558484
23andMe allrs72558484
SNP Nexus

SNPshotrs72558484
SNPdbers72558484
MSV3drs72558484
GWAS Ctlgrs72558484
Max Magnitude0
ClinVar
Risk rs72558484(C;C)
Alt rs72558484(C;C)
Reference rs72558484(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271254T>C
CLNSRC ClinVar
CLNACC RCV000083314.1,