Have questions? Visit https://www.reddit.com/r/SNPedia

rs66642398

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs66642398(A;A)
Make rs66642398(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403663
GeneOTC
is asnp
is mentioned by
dbSNPrs66642398
ebirs66642398
HLIrs66642398
Exacrs66642398
Varsomers66642398
Maprs66642398
PheGenIrs66642398
hapmaprs66642398
1000 genomesrs66642398
hgdprs66642398
ensemblrs66642398
gopubmedrs66642398
geneviewrs66642398
scholarrs66642398
googlers66642398
pharmgkbrs66642398
gwascentralrs66642398
openSNPrs66642398
23andMers66642398
23andMe allrs66642398
SNP Nexus

SNPshotrs66642398
SNPdbers66642398
MSV3drs66642398
GWAS Ctlgrs66642398
Max Magnitude0
ClinVar
Risk rs66642398(A,T;A,T)
Alt rs66642398(A,T;A,T)
Reference rs66642398(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262916G>A; NC_000023.10:g.38262916G>T
CLNSRC ClinVar
CLNACC RCV000083499.1, RCV000083500.1,



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


[PMID 9686344] The biochemical and molecular spectrum of ornithine transcarbamylase deficiency.