Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225057

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225057(G;G)
Make rs863225057(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128879693
GeneACAD9
is asnp
is mentioned by
dbSNPrs863225057
ebirs863225057
HLIrs863225057
Exacrs863225057
Varsomers863225057
Maprs863225057
PheGenIrs863225057
hapmaprs863225057
1000 genomesrs863225057
hgdprs863225057
ensemblrs863225057
gopubmedrs863225057
geneviewrs863225057
scholarrs863225057
googlers863225057
pharmgkbrs863225057
gwascentralrs863225057
openSNPrs863225057
23andMers863225057
23andMe allrs863225057
SNP Nexus

SNPshotrs863225057
SNPdbers863225057
MSV3drs863225057
GWAS Ctlgrs863225057
Max Magnitude0
ClinVar
Risk rs863225057(G;G)
Alt rs863225057(G;G)
Reference rs863225057(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.128598536T>G
CLNSRC
CLNACC RCV000201549.1,