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rs72558461

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558461(C;C)
Make rs72558461(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411887
GeneOTC
is asnp
is mentioned by
dbSNPrs72558461
ebirs72558461
HLIrs72558461
Exacrs72558461
Varsomers72558461
Maprs72558461
PheGenIrs72558461
hapmaprs72558461
1000 genomesrs72558461
hgdprs72558461
ensemblrs72558461
gopubmedrs72558461
geneviewrs72558461
scholarrs72558461
googlers72558461
pharmgkbrs72558461
gwascentralrs72558461
openSNPrs72558461
23andMers72558461
23andMe allrs72558461
SNP Nexus

SNPshotrs72558461
SNPdbers72558461
MSV3drs72558461
GWAS Ctlgrs72558461
Max Magnitude0
ClinVar
Risk rs72558461(C;C)
Alt rs72558461(C;C)
Reference rs72558461(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271140G>C
CLNSRC ClinVar
CLNACC RCV000083597.1,