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rs387907041

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907041(A;A)
Make rs387907041(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position128879821
GeneACAD9
is asnp
is mentioned by
dbSNPrs387907041
ebirs387907041
HLIrs387907041
Exacrs387907041
Varsomers387907041
Maprs387907041
PheGenIrs387907041
hapmaprs387907041
1000 genomesrs387907041
hgdprs387907041
ensemblrs387907041
gopubmedrs387907041
geneviewrs387907041
scholarrs387907041
googlers387907041
pharmgkbrs387907041
gwascentralrs387907041
openSNPrs387907041
23andMers387907041
23andMe allrs387907041
SNP Nexus

SNPshotrs387907041
SNPdbers387907041
MSV3drs387907041
GWAS Ctlgrs387907041
Max Magnitude0
ClinVar
Risk rs387907041(A;A)
Alt rs387907041(A;A)
Reference rs387907041(T;T)
Significance Pathogenic
Disease Acyl-CoA dehydrogenase family
Variation info
Gene ACAD9
CLNDBN Acyl-CoA dehydrogenase family, member 9, deficiency of
Reversed 0
HGVS NC_000003.11:g.128598664T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023866.2,