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rs67330615

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs67330615(A;A)
Make rs67330615(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408915
GeneOTC
is asnp
is mentioned by
dbSNPrs67330615
ebirs67330615
HLIrs67330615
Exacrs67330615
Varsomers67330615
Maprs67330615
PheGenIrs67330615
hapmaprs67330615
1000 genomesrs67330615
hgdprs67330615
ensemblrs67330615
gopubmedrs67330615
geneviewrs67330615
scholarrs67330615
googlers67330615
pharmgkbrs67330615
gwascentralrs67330615
openSNPrs67330615
23andMers67330615
23andMe allrs67330615
SNP Nexus

SNPshotrs67330615
SNPdbers67330615
MSV3drs67330615
GWAS Ctlgrs67330615
Max Magnitude0
ClinVar
Risk rs67330615(A,C;A,C)
Alt rs67330615(A,C;A,C)
Reference rs67330615(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268168G>A; NC_000023.10:g.38268168G>C
CLNSRC ClinVar
CLNACC RCV000083555.1, RCV000083556.1,



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