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rs72558463

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558463(C;T)
Make rs72558463(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411898
GeneOTC
is asnp
is mentioned by
dbSNPrs72558463
ebirs72558463
HLIrs72558463
Exacrs72558463
Varsomers72558463
Maprs72558463
PheGenIrs72558463
hapmaprs72558463
1000 genomesrs72558463
hgdprs72558463
ensemblrs72558463
gopubmedrs72558463
geneviewrs72558463
scholarrs72558463
googlers72558463
pharmgkbrs72558463
gwascentralrs72558463
openSNPrs72558463
23andMers72558463
23andMe allrs72558463
SNP Nexus

SNPshotrs72558463
SNPdbers72558463
MSV3drs72558463
GWAS Ctlgrs72558463
Max Magnitude0
ClinVar
Risk rs72558463(T;T)
Alt rs72558463(T;T)
Reference rs72558463(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271151C>T
CLNSRC ClinVar
CLNACC RCV000083599.1,