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rs72558409

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558409(A;C)
Make rs72558409(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403682
GeneOTC
is asnp
is mentioned by
dbSNPrs72558409
ebirs72558409
HLIrs72558409
Exacrs72558409
Varsomers72558409
Maprs72558409
PheGenIrs72558409
hapmaprs72558409
1000 genomesrs72558409
hgdprs72558409
ensemblrs72558409
gopubmedrs72558409
geneviewrs72558409
scholarrs72558409
googlers72558409
pharmgkbrs72558409
gwascentralrs72558409
openSNPrs72558409
23andMers72558409
23andMe allrs72558409
SNP Nexus

SNPshotrs72558409
SNPdbers72558409
MSV3drs72558409
GWAS Ctlgrs72558409
Max Magnitude0
ClinVar
Risk rs72558409(C;C)
Alt rs72558409(C;C)
Reference rs72558409(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262935A>C
CLNSRC ClinVar
CLNACC RCV000083510.1,