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rs863224845

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224845(C;T)
Make rs863224845(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128912587
GeneACAD9, KIAA1257
is asnp
is mentioned by
dbSNPrs863224845
ebirs863224845
HLIrs863224845
Exacrs863224845
Varsomers863224845
Maprs863224845
PheGenIrs863224845
hapmaprs863224845
1000 genomesrs863224845
hgdprs863224845
ensemblrs863224845
gopubmedrs863224845
geneviewrs863224845
scholarrs863224845
googlers863224845
pharmgkbrs863224845
gwascentralrs863224845
openSNPrs863224845
23andMers863224845
23andMe allrs863224845
SNP Nexus

SNPshotrs863224845
SNPdbers863224845
MSV3drs863224845
GWAS Ctlgrs863224845
Max Magnitude0
ClinVar
Risk rs863224845(T;T)
Alt rs863224845(T;T)
Reference rs863224845(C;C)
Significance Probable-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.128631430C>T
CLNSRC
CLNACC RCV000199949.1,