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rs863224844

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224844(-;-)
Make rs863224844(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128895322
GeneACAD9
is asnp
is mentioned by
dbSNPrs863224844
dbSNP (classic)rs863224844
ClinGenrs863224844
ebirs863224844
HLIrs863224844
Exacrs863224844
Gnomadrs863224844
Varsomers863224844
LitVarrs863224844
Maprs863224844
PheGenIrs863224844
Biobankrs863224844
1000 genomesrs863224844
hgdprs863224844
ensemblrs863224844
geneviewrs863224844
scholarrs863224844
googlers863224844
pharmgkbrs863224844
gwascentralrs863224844
openSNPrs863224844
23andMers863224844
SNPshotrs863224844
SNPdbers863224844
MSV3drs863224844
GWAS Ctlgrs863224844
Max Magnitude0
ClinVar
Risk rs863224844(-;-)
Alt rs863224844(-;-)
Reference Rs863224844(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.128614165delT
CLNSRC
CLNACC RCV000199949.1, RCV000201606.1,