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rs150283105

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150283105(C;T)
Make rs150283105(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128909410
GeneACAD9
is asnp
is mentioned by
dbSNPrs150283105
dbSNP (classic)rs150283105
ClinGenrs150283105
ebirs150283105
HLIrs150283105
Exacrs150283105
Gnomadrs150283105
Varsomers150283105
LitVarrs150283105
Maprs150283105
PheGenIrs150283105
Biobankrs150283105
1000 genomesrs150283105
hgdprs150283105
ensemblrs150283105
geneviewrs150283105
scholarrs150283105
googlers150283105
pharmgkbrs150283105
gwascentralrs150283105
openSNPrs150283105
23andMers150283105
SNPshotrs150283105
SNPdbers150283105
MSV3drs150283105
GWAS Ctlgrs150283105
Max Magnitude0
ClinVar
Risk rs150283105(T;T)
Alt rs150283105(T;T)
Reference Rs150283105(C;C)
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.128628253C>T
CLNSRC
CLNACC RCV000201643.1, RCV000201736.1,