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rs66521141

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs66521141(A;A)
Make rs66521141(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367367
GeneOTC
is asnp
is mentioned by
dbSNPrs66521141
ebirs66521141
HLIrs66521141
Exacrs66521141
Varsomers66521141
Maprs66521141
PheGenIrs66521141
hapmaprs66521141
1000 genomesrs66521141
hgdprs66521141
ensemblrs66521141
gopubmedrs66521141
geneviewrs66521141
scholarrs66521141
googlers66521141
pharmgkbrs66521141
gwascentralrs66521141
openSNPrs66521141
23andMers66521141
23andMe allrs66521141
SNP Nexus

SNPshotrs66521141
SNPdbers66521141
MSV3drs66521141
GWAS Ctlgrs66521141
Max Magnitude0
ClinVar
Risk rs66521141(A,T;A,T)
Alt rs66521141(A,T;A,T)
Reference rs66521141(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226620G>A; NC_000023.10:g.38226620G>T
CLNSRC ClinVar
CLNACC RCV000083347.1, RCV000083348.1,


[PMID 10946359] Genotype spectrum of ornithine transcarbamylase deficiency: correlation with the clinical and biochemical phenotype.