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rs121965034

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121965034(A;A)
Make rs121965034(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position124412169
GeneOAT
is asnp
is mentioned by
dbSNPrs121965034
ebirs121965034
HLIrs121965034
Exacrs121965034
Varsomers121965034
Maprs121965034
PheGenIrs121965034
hapmaprs121965034
1000 genomesrs121965034
hgdprs121965034
ensemblrs121965034
gopubmedrs121965034
geneviewrs121965034
scholarrs121965034
googlers121965034
pharmgkbrs121965034
gwascentralrs121965034
openSNPrs121965034
23andMers121965034
23andMe allrs121965034
SNP Nexus

SNPshotrs121965034
SNPdbers121965034
MSV3drs121965034
GWAS Ctlgrs121965034
Max Magnitude0
OMIM613349
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121965034(A;A)
Alt rs121965034(A;A)
Reference rs121965034(G;G)
Significance Pathogenic
Disease Ornithine aminotransferase deficiency
Variation info
Gene OAT
CLNDBN Ornithine aminotransferase deficiency
Reversed 1
HGVS NC_000010.10:g.126100738C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000169.2,