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rs863225058

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225058(A;G)
Make rs863225058(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128884651
GeneACAD9
is asnp
is mentioned by
dbSNPrs863225058
ebirs863225058
HLIrs863225058
Exacrs863225058
Varsomers863225058
Maprs863225058
PheGenIrs863225058
hapmaprs863225058
1000 genomesrs863225058
hgdprs863225058
ensemblrs863225058
gopubmedrs863225058
geneviewrs863225058
scholarrs863225058
googlers863225058
pharmgkbrs863225058
gwascentralrs863225058
openSNPrs863225058
23andMers863225058
23andMe allrs863225058
SNP Nexus

SNPshotrs863225058
SNPdbers863225058
MSV3drs863225058
GWAS Ctlgrs863225058
Max Magnitude0
ClinVar
Risk rs863225058(G;G)
Alt rs863225058(G;G)
Reference rs863225058(A;A)
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.128603494A>G
CLNSRC
CLNACC RCV000201557.1,