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rs72558406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558406(A;G)
Make rs72558406(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403673
GeneOTC
is asnp
is mentioned by
dbSNPrs72558406
ebirs72558406
HLIrs72558406
Exacrs72558406
Varsomers72558406
Maprs72558406
PheGenIrs72558406
hapmaprs72558406
1000 genomesrs72558406
hgdprs72558406
ensemblrs72558406
gopubmedrs72558406
geneviewrs72558406
scholarrs72558406
googlers72558406
pharmgkbrs72558406
gwascentralrs72558406
openSNPrs72558406
23andMers72558406
23andMe allrs72558406
SNP Nexus

SNPshotrs72558406
SNPdbers72558406
MSV3drs72558406
GWAS Ctlgrs72558406
Max Magnitude0
ClinVar
Risk rs72558406(G;G)
Alt rs72558406(G;G)
Reference rs72558406(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262926A>G
CLNSRC ClinVar
CLNACC RCV000083507.1,