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rs72558413

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558413(C;C)
Make rs72558413(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403695
GeneOTC
is asnp
is mentioned by
dbSNPrs72558413
ebirs72558413
HLIrs72558413
Exacrs72558413
Varsomers72558413
Maprs72558413
PheGenIrs72558413
hapmaprs72558413
1000 genomesrs72558413
hgdprs72558413
ensemblrs72558413
gopubmedrs72558413
geneviewrs72558413
scholarrs72558413
googlers72558413
pharmgkbrs72558413
gwascentralrs72558413
openSNPrs72558413
23andMers72558413
23andMe allrs72558413
SNP Nexus

SNPshotrs72558413
SNPdbers72558413
MSV3drs72558413
GWAS Ctlgrs72558413
Max Magnitude0
ClinVar
Risk rs72558413(C;C)
Alt rs72558413(C;C)
Reference rs72558413(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262948G>C
CLNSRC ClinVar
CLNACC RCV000083514.1,