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rs72558493

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558493(A;A)
Make rs72558493(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421056
GeneOTC
is asnp
is mentioned by
dbSNPrs72558493
ebirs72558493
HLIrs72558493
Exacrs72558493
Varsomers72558493
Maprs72558493
PheGenIrs72558493
hapmaprs72558493
1000 genomesrs72558493
hgdprs72558493
ensemblrs72558493
gopubmedrs72558493
geneviewrs72558493
scholarrs72558493
googlers72558493
pharmgkbrs72558493
gwascentralrs72558493
openSNPrs72558493
23andMers72558493
23andMe allrs72558493
SNP Nexus

SNPshotrs72558493
SNPdbers72558493
MSV3drs72558493
GWAS Ctlgrs72558493
Max Magnitude0
ClinVar
Risk rs72558493(A;A)
Alt rs72558493(A;A)
Reference rs72558493(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280309C>A
CLNSRC ClinVar
CLNACC RCV000083327.1,