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rs72558481

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558481(A;A)
Make rs72558481(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411989
GeneOTC
is asnp
is mentioned by
dbSNPrs72558481
ebirs72558481
HLIrs72558481
Exacrs72558481
Varsomers72558481
Maprs72558481
PheGenIrs72558481
hapmaprs72558481
1000 genomesrs72558481
hgdprs72558481
ensemblrs72558481
gopubmedrs72558481
geneviewrs72558481
scholarrs72558481
googlers72558481
pharmgkbrs72558481
gwascentralrs72558481
openSNPrs72558481
23andMers72558481
23andMe allrs72558481
SNP Nexus

SNPshotrs72558481
SNPdbers72558481
MSV3drs72558481
GWAS Ctlgrs72558481
Max Magnitude0
ClinVar
Risk rs72558481(A;A)
Alt rs72558481(A;A)
Reference rs72558481(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271242G>A
CLNSRC ClinVar
CLNACC RCV000083628.1,