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rs72558404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558404(A;A)
Make rs72558404(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403671
GeneOTC
is asnp
is mentioned by
dbSNPrs72558404
ebirs72558404
HLIrs72558404
Exacrs72558404
Varsomers72558404
Maprs72558404
PheGenIrs72558404
hapmaprs72558404
1000 genomesrs72558404
hgdprs72558404
ensemblrs72558404
gopubmedrs72558404
geneviewrs72558404
scholarrs72558404
googlers72558404
pharmgkbrs72558404
gwascentralrs72558404
openSNPrs72558404
23andMers72558404
23andMe allrs72558404
SNP Nexus

SNPshotrs72558404
SNPdbers72558404
MSV3drs72558404
GWAS Ctlgrs72558404
Max Magnitude0
ClinVar
Risk rs72558404(A;A)
Alt rs72558404(A;A)
Reference rs72558404(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262924C>A
CLNSRC ClinVar
CLNACC RCV000083505.1,