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rs863225056

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225056(G;G)
Make rs863225056(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128904118
GeneACAD9
is asnp
is mentioned by
dbSNPrs863225056
ebirs863225056
HLIrs863225056
Exacrs863225056
Varsomers863225056
Maprs863225056
PheGenIrs863225056
hapmaprs863225056
1000 genomesrs863225056
hgdprs863225056
ensemblrs863225056
gopubmedrs863225056
geneviewrs863225056
scholarrs863225056
googlers863225056
pharmgkbrs863225056
gwascentralrs863225056
openSNPrs863225056
23andMers863225056
23andMe allrs863225056
SNP Nexus

SNPshotrs863225056
SNPdbers863225056
MSV3drs863225056
GWAS Ctlgrs863225056
Max Magnitude0
ClinVar
Risk rs863225056(G;G)
Alt rs863225056(G;G)
Reference rs863225056(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.128622961T>G
CLNSRC
CLNACC RCV000201549.1,