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rs387906242

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs387906242(-;-)
Make rs387906242(-;TAAG)
Make rs387906242(TAAG;TAAG)
ReferenceGRCh38 38.1/141
Chromosome3
Position128879651
GeneACAD9
is asnp
is mentioned by
dbSNPrs387906242
ebirs387906242
HLIrs387906242
Exacrs387906242
Varsomers387906242
Maprs387906242
PheGenIrs387906242
hapmaprs387906242
1000 genomesrs387906242
hgdprs387906242
ensemblrs387906242
gopubmedrs387906242
geneviewrs387906242
scholarrs387906242
googlers387906242
pharmgkbrs387906242
gwascentralrs387906242
openSNPrs387906242
23andMers387906242
23andMe allrs387906242
SNP Nexus

SNPshotrs387906242
SNPdbers387906242
MSV3drs387906242
GWAS Ctlgrs387906242
GMAF0.0528
Max Magnitude0
ClinVar
Risk rs387906242(TAAG;TAAG)
Alt rs387906242(TAAG;TAAG)
Reference rs387906242(;)
Significance Pathogenic
Disease Acyl-CoA dehydrogenase family not specified
Variation info
Gene ACAD9
CLNDBN Acyl-CoA dehydrogenase family, member 9, deficiency of not specified
Reversed 0
HGVS NC_000003.11:g.128598491_128598494dupTAAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000001073.3, RCV000201519.1,