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rs66724222

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs66724222(A;A)
Make rs66724222(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408988
GeneOTC
is asnp
is mentioned by
dbSNPrs66724222
ebirs66724222
HLIrs66724222
Exacrs66724222
Varsomers66724222
Maprs66724222
PheGenIrs66724222
hapmaprs66724222
1000 genomesrs66724222
hgdprs66724222
ensemblrs66724222
gopubmedrs66724222
geneviewrs66724222
scholarrs66724222
googlers66724222
pharmgkbrs66724222
gwascentralrs66724222
openSNPrs66724222
23andMers66724222
23andMe allrs66724222
SNP Nexus

SNPshotrs66724222
SNPdbers66724222
MSV3drs66724222
GWAS Ctlgrs66724222
Max Magnitude0
ClinVar
Risk rs66724222(A,T;A,T)
Alt rs66724222(A,T;A,T)
Reference rs66724222(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268241G>A; NC_000023.10:g.38268241G>T
CLNSRC ClinVar
CLNACC RCV000083587.1, RCV000083588.1,



[PMID 7951259] Seven new mutations in the human ornithine transcarbamylase gene.


[PMID 11793468] Mutations and polymorphisms in the human ornithine transcarbamylase gene.