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rs72558440

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558440(A;C)
Make rs72558440(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408922
GeneOTC
is asnp
is mentioned by
dbSNPrs72558440
ebirs72558440
HLIrs72558440
Exacrs72558440
Varsomers72558440
Maprs72558440
PheGenIrs72558440
hapmaprs72558440
1000 genomesrs72558440
hgdprs72558440
ensemblrs72558440
gopubmedrs72558440
geneviewrs72558440
scholarrs72558440
googlers72558440
pharmgkbrs72558440
gwascentralrs72558440
openSNPrs72558440
23andMers72558440
23andMe allrs72558440
SNP Nexus

SNPshotrs72558440
SNPdbers72558440
MSV3drs72558440
GWAS Ctlgrs72558440
Max Magnitude0
ClinVar
Risk rs72558440(C,G;C,G)
Alt rs72558440(C,G;C,G)
Reference rs72558440(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268175A>C
CLNSRC ClinVar
CLNACC RCV000083558.1,