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rs267606924

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606924(A;A)
Make rs267606924(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position124403003
GeneOAT
is asnp
is mentioned by
dbSNPrs267606924
ebirs267606924
HLIrs267606924
Exacrs267606924
Varsomers267606924
Maprs267606924
PheGenIrs267606924
hapmaprs267606924
1000 genomesrs267606924
hgdprs267606924
ensemblrs267606924
gopubmedrs267606924
geneviewrs267606924
scholarrs267606924
googlers267606924
pharmgkbrs267606924
gwascentralrs267606924
openSNPrs267606924
23andMers267606924
23andMe allrs267606924
SNP Nexus

SNPshotrs267606924
SNPdbers267606924
MSV3drs267606924
GWAS Ctlgrs267606924
Max Magnitude0
ClinVar
Risk rs267606924(A;A)
Alt rs267606924(A;A)
Reference rs267606924(G;G)
Significance Pathogenic
Disease Ornithine aminotransferase deficiency
Variation info
Gene OAT
CLNDBN Ornithine aminotransferase deficiency
Reversed 1
HGVS NC_000010.10:g.126091572C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000203.2,