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rs863225059

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCCCAGACCATC;TCCCAGACCATC) 0 common in clinvar
Make rs863225059(-;-)
Make rs863225059(-;TCCCAGACCATC)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128910015
GeneACAD9, KIAA1257
is asnp
is mentioned by
dbSNPrs863225059
ClinGenrs863225059
ebirs863225059
HLIrs863225059
Exacrs863225059
Varsomers863225059
Maprs863225059
PheGenIrs863225059
hapmaprs863225059
1000 genomesrs863225059
hgdprs863225059
ensemblrs863225059
gopubmedrs863225059
geneviewrs863225059
scholarrs863225059
googlers863225059
pharmgkbrs863225059
gwascentralrs863225059
openSNPrs863225059
23andMers863225059
23andMe allrs863225059
SNP Nexus

SNPshotrs863225059
SNPdbers863225059
MSV3drs863225059
GWAS Ctlgrs863225059
Max Magnitude0
ClinVar
Risk rs863225059(-;-)
Alt rs863225059(-;-)
Reference Rs863225059(TCCCAGACCATC;TCCCAGACCATC)
Significance Pathogenic
Disease Acyl-CoA dehydrogenase family
Variation info
Gene LOC100132731 ACAD9
CLNDBN Acyl-CoA dehydrogenase family, member 9, deficiency of
Reversed 0
HGVS NC_000003.11:g.128628858_128628869delTCCCAGACCATC
CLNSRC
CLNACC RCV000201736.1,