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rs72558467

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558467(A;G)
Make rs72558467(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411923
GeneOTC
is asnp
is mentioned by
dbSNPrs72558467
ClinGenrs72558467
ebirs72558467
HLIrs72558467
Exacrs72558467
Varsomers72558467
Maprs72558467
PheGenIrs72558467
hapmaprs72558467
1000 genomesrs72558467
hgdprs72558467
ensemblrs72558467
gopubmedrs72558467
geneviewrs72558467
scholarrs72558467
googlers72558467
pharmgkbrs72558467
gwascentralrs72558467
openSNPrs72558467
23andMers72558467
23andMe allrs72558467
SNP Nexus

SNPshotrs72558467
SNPdbers72558467
MSV3drs72558467
GWAS Ctlgrs72558467
Max Magnitude0
ClinVar
Risk rs72558467(G;G)
Alt rs72558467(G;G)
Reference Rs72558467(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271176A>G
CLNSRC ClinVar
CLNACC RCV000083611.1,