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rs66677059

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs66677059(C;C)
Make rs66677059(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367371
GeneOTC
is asnp
is mentioned by
dbSNPrs66677059
ebirs66677059
HLIrs66677059
Exacrs66677059
Varsomers66677059
Maprs66677059
PheGenIrs66677059
hapmaprs66677059
1000 genomesrs66677059
hgdprs66677059
ensemblrs66677059
gopubmedrs66677059
geneviewrs66677059
scholarrs66677059
googlers66677059
pharmgkbrs66677059
gwascentralrs66677059
openSNPrs66677059
23andMers66677059
23andMe allrs66677059
SNP Nexus

SNPshotrs66677059
SNPdbers66677059
MSV3drs66677059
GWAS Ctlgrs66677059
Max Magnitude0
ClinVar
Risk rs66677059(C,G;C,G)
Alt rs66677059(C,G;C,G)
Reference rs66677059(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226624T>C; NC_000023.10:g.38226624T>G
CLNSRC ClinVar
CLNACC RCV000083351.1, RCV000083352.1,



[PMID 16786505] Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene.