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rs387907042

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907042(A;A)
Make rs387907042(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position128899450
GeneACAD9
is asnp
is mentioned by
dbSNPrs387907042
ebirs387907042
HLIrs387907042
Exacrs387907042
Varsomers387907042
Maprs387907042
PheGenIrs387907042
hapmaprs387907042
1000 genomesrs387907042
hgdprs387907042
ensemblrs387907042
gopubmedrs387907042
geneviewrs387907042
scholarrs387907042
googlers387907042
pharmgkbrs387907042
gwascentralrs387907042
openSNPrs387907042
23andMers387907042
23andMe allrs387907042
SNP Nexus

SNPshotrs387907042
SNPdbers387907042
MSV3drs387907042
GWAS Ctlgrs387907042
Max Magnitude0
ClinVar
Risk rs387907042(A;A)
Alt rs387907042(A;A)
Reference rs387907042(G;G)
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.128618293G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023867.3,