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rs267606925

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606925(A;A)
Make rs267606925(A;C)
ReferenceGRCh38 38.1/141
Chromosome10
Position124405488
GeneOAT
is asnp
is mentioned by
dbSNPrs267606925
ebirs267606925
HLIrs267606925
Exacrs267606925
Varsomers267606925
Maprs267606925
PheGenIrs267606925
hapmaprs267606925
1000 genomesrs267606925
hgdprs267606925
ensemblrs267606925
gopubmedrs267606925
geneviewrs267606925
scholarrs267606925
googlers267606925
pharmgkbrs267606925
gwascentralrs267606925
openSNPrs267606925
23andMers267606925
23andMe allrs267606925
SNP Nexus

SNPshotrs267606925
SNPdbers267606925
MSV3drs267606925
GWAS Ctlgrs267606925
Max Magnitude0
ClinVar
Risk rs267606925(A;A)
Alt rs267606925(A;A)
Reference rs267606925(C;C)
Significance Pathogenic
Disease Ornithine aminotransferase deficiency
Variation info
Gene OAT
CLNDBN Ornithine aminotransferase deficiency
Reversed 1
HGVS NC_000010.10:g.126094057G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000206.2,