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rs72558410

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558410(C;G)
Make rs72558410(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403685
GeneOTC
is asnp
is mentioned by
dbSNPrs72558410
ebirs72558410
HLIrs72558410
Exacrs72558410
Varsomers72558410
Maprs72558410
PheGenIrs72558410
hapmaprs72558410
1000 genomesrs72558410
hgdprs72558410
ensemblrs72558410
gopubmedrs72558410
geneviewrs72558410
scholarrs72558410
googlers72558410
pharmgkbrs72558410
gwascentralrs72558410
openSNPrs72558410
23andMers72558410
23andMe allrs72558410
SNP Nexus

SNPshotrs72558410
SNPdbers72558410
MSV3drs72558410
GWAS Ctlgrs72558410
Max Magnitude0
ClinVar
Risk rs72558410(G;G)
Alt rs72558410(G;G)
Reference rs72558410(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262938C>G
CLNSRC ClinVar
CLNACC RCV000083511.1,