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rs72558466

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558466(G;T)
Make rs72558466(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411922
GeneOTC
is asnp
is mentioned by
dbSNPrs72558466
ebirs72558466
HLIrs72558466
Exacrs72558466
Varsomers72558466
Maprs72558466
PheGenIrs72558466
hapmaprs72558466
1000 genomesrs72558466
hgdprs72558466
ensemblrs72558466
gopubmedrs72558466
geneviewrs72558466
scholarrs72558466
googlers72558466
pharmgkbrs72558466
gwascentralrs72558466
openSNPrs72558466
23andMers72558466
23andMe allrs72558466
SNP Nexus

SNPshotrs72558466
SNPdbers72558466
MSV3drs72558466
GWAS Ctlgrs72558466
Max Magnitude0
ClinVar
Risk rs72558466(T;T)
Alt rs72558466(T;T)
Reference rs72558466(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271175G>T
CLNSRC ClinVar
CLNACC RCV000083610.1,