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rs72558450

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558450(A;A)
Make rs72558450(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408964
GeneOTC
is asnp
is mentioned by
dbSNPrs72558450
ebirs72558450
HLIrs72558450
Exacrs72558450
Varsomers72558450
Maprs72558450
PheGenIrs72558450
hapmaprs72558450
1000 genomesrs72558450
hgdprs72558450
ensemblrs72558450
gopubmedrs72558450
geneviewrs72558450
scholarrs72558450
googlers72558450
pharmgkbrs72558450
gwascentralrs72558450
openSNPrs72558450
23andMers72558450
23andMe allrs72558450
SNP Nexus

SNPshotrs72558450
SNPdbers72558450
MSV3drs72558450
GWAS Ctlgrs72558450
Max Magnitude0
ClinVar
Risk rs72558450(A;A)
Alt rs72558450(A;A)
Reference rs72558450(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268217G>A
CLNSRC ClinVar
CLNACC RCV000083581.1,