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rs72558443

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558443(A;G)
Make rs72558443(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408946
GeneOTC
is asnp
is mentioned by
dbSNPrs72558443
ebirs72558443
HLIrs72558443
Exacrs72558443
Varsomers72558443
Maprs72558443
PheGenIrs72558443
hapmaprs72558443
1000 genomesrs72558443
hgdprs72558443
ensemblrs72558443
gopubmedrs72558443
geneviewrs72558443
scholarrs72558443
googlers72558443
pharmgkbrs72558443
gwascentralrs72558443
openSNPrs72558443
23andMers72558443
23andMe allrs72558443
SNP Nexus

SNPshotrs72558443
SNPdbers72558443
MSV3drs72558443
GWAS Ctlgrs72558443
Max Magnitude0
ClinVar
Risk rs72558443(G;G)
Alt rs72558443(G;G)
Reference rs72558443(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268199A>G
CLNSRC ClinVar
CLNACC RCV000083572.1,