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rs121965050

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121965050(A;A)
Make rs121965050(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position124405534
GeneOAT
is asnp
is mentioned by
dbSNPrs121965050
ebirs121965050
HLIrs121965050
Exacrs121965050
Varsomers121965050
Maprs121965050
PheGenIrs121965050
hapmaprs121965050
1000 genomesrs121965050
hgdprs121965050
ensemblrs121965050
gopubmedrs121965050
geneviewrs121965050
scholarrs121965050
googlers121965050
pharmgkbrs121965050
gwascentralrs121965050
openSNPrs121965050
23andMers121965050
23andMe allrs121965050
SNP Nexus

SNPshotrs121965050
SNPdbers121965050
MSV3drs121965050
GWAS Ctlgrs121965050
Max Magnitude0
OMIM613349
Desc
Variant0024
Relatedalso
ClinVar
Risk rs121965050(A;A)
Alt rs121965050(A;A)
Reference rs121965050(G;G)
Significance Pathogenic
Disease Ornithine aminotransferase deficiency
Variation info
Gene OAT
CLNDBN Ornithine aminotransferase deficiency
Reversed 1
HGVS NC_000010.10:g.126094103C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000190.2,