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rs67284661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs67284661(C;C)
Make rs67284661(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403654
GeneOTC
is asnp
is mentioned by
dbSNPrs67284661
ebirs67284661
HLIrs67284661
Exacrs67284661
Varsomers67284661
Maprs67284661
PheGenIrs67284661
hapmaprs67284661
1000 genomesrs67284661
hgdprs67284661
ensemblrs67284661
gopubmedrs67284661
geneviewrs67284661
scholarrs67284661
googlers67284661
pharmgkbrs67284661
gwascentralrs67284661
openSNPrs67284661
23andMers67284661
23andMe allrs67284661
SNP Nexus

SNPshotrs67284661
SNPdbers67284661
MSV3drs67284661
GWAS Ctlgrs67284661
Max Magnitude0
ClinVar
Risk rs67284661(C,G;C,G)
Alt rs67284661(C,G;C,G)
Reference rs67284661(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262907T>C; NC_000023.10:g.38262907T>G
CLNSRC ClinVar
CLNACC RCV000083494.1, RCV000083495.1,



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