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rs66737144

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs66737144(G;T)
Make rs66737144(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38381430
GeneOTC
is asnp
is mentioned by
dbSNPrs66737144
ebirs66737144
HLIrs66737144
Exacrs66737144
Varsomers66737144
Maprs66737144
PheGenIrs66737144
hapmaprs66737144
1000 genomesrs66737144
hgdprs66737144
ensemblrs66737144
gopubmedrs66737144
geneviewrs66737144
scholarrs66737144
googlers66737144
pharmgkbrs66737144
gwascentralrs66737144
openSNPrs66737144
23andMers66737144
23andMe allrs66737144
SNP Nexus

SNPshotrs66737144
SNPdbers66737144
MSV3drs66737144
GWAS Ctlgrs66737144
Max Magnitude0
ClinVar
Risk rs66737144(A,T;A,T)
Alt rs66737144(A,T;A,T)
Reference rs66737144(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38240683G>A; NC_000023.10:g.38240683G>T
CLNSRC ClinVar
CLNACC RCV000083411.1, RCV000083412.1,



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