Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606923

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606923(A;A)
Make rs267606923(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position124405551
GeneOAT
is asnp
is mentioned by
dbSNPrs267606923
ebirs267606923
HLIrs267606923
Exacrs267606923
Varsomers267606923
Maprs267606923
PheGenIrs267606923
hapmaprs267606923
1000 genomesrs267606923
hgdprs267606923
ensemblrs267606923
gopubmedrs267606923
geneviewrs267606923
scholarrs267606923
googlers267606923
pharmgkbrs267606923
gwascentralrs267606923
openSNPrs267606923
23andMers267606923
23andMe allrs267606923
SNP Nexus

SNPshotrs267606923
SNPdbers267606923
MSV3drs267606923
GWAS Ctlgrs267606923
Max Magnitude0
ClinVar
Risk rs267606923(A;A)
Alt rs267606923(A;A)
Reference rs267606923(G;G)
Significance Pathogenic
Disease Ornithine aminotransferase deficiency
Variation info
Gene OAT
CLNDBN Ornithine aminotransferase deficiency
Reversed 1
HGVS NC_000010.10:g.126094120C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000202.2,