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rs67333670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs67333670(A;A)
Make rs67333670(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408943
GeneOTC
is asnp
is mentioned by
dbSNPrs67333670
ebirs67333670
HLIrs67333670
Exacrs67333670
Varsomers67333670
Maprs67333670
PheGenIrs67333670
hapmaprs67333670
1000 genomesrs67333670
hgdprs67333670
ensemblrs67333670
gopubmedrs67333670
geneviewrs67333670
scholarrs67333670
googlers67333670
pharmgkbrs67333670
gwascentralrs67333670
openSNPrs67333670
23andMers67333670
23andMe allrs67333670
SNP Nexus

SNPshotrs67333670
SNPdbers67333670
MSV3drs67333670
GWAS Ctlgrs67333670
Max Magnitude0
ClinVar
Risk rs67333670(A,T;A,T)
Alt rs67333670(A,T;A,T)
Reference rs67333670(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268196C>A; NC_000023.10:g.38268196C>T
CLNSRC ClinVar
CLNACC RCV000083569.1, RCV000083570.1,



[PMID 10737985] Lymphocyte mRNA analysis of the ornithine transcarbamylase gene in Italian OTCD male patients and manifesting carriers: identification of novel mutations.


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