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rs72558433

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558433(A;G)
Make rs72558433(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408874
GeneOTC
is asnp
is mentioned by
dbSNPrs72558433
ebirs72558433
HLIrs72558433
Exacrs72558433
Varsomers72558433
Maprs72558433
PheGenIrs72558433
hapmaprs72558433
1000 genomesrs72558433
hgdprs72558433
ensemblrs72558433
gopubmedrs72558433
geneviewrs72558433
scholarrs72558433
googlers72558433
pharmgkbrs72558433
gwascentralrs72558433
openSNPrs72558433
23andMers72558433
23andMe allrs72558433
SNP Nexus

SNPshotrs72558433
SNPdbers72558433
MSV3drs72558433
GWAS Ctlgrs72558433
Max Magnitude0
ClinVar
Risk rs72558433(G;G)
Alt rs72558433(G;G)
Reference rs72558433(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268127A>G
CLNSRC ClinVar
CLNACC RCV000083549.1,