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rs773586510

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs773586510(G;T)
Make rs773586510(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128904385
GeneACAD9
is asnp
is mentioned by
dbSNPrs773586510
ebirs773586510
HLIrs773586510
Exacrs773586510
Varsomers773586510
Maprs773586510
PheGenIrs773586510
hapmaprs773586510
1000 genomesrs773586510
hgdprs773586510
ensemblrs773586510
gopubmedrs773586510
geneviewrs773586510
scholarrs773586510
googlers773586510
pharmgkbrs773586510
gwascentralrs773586510
openSNPrs773586510
23andMers773586510
23andMe allrs773586510
SNP Nexus

SNPshotrs773586510
SNPdbers773586510
MSV3drs773586510
GWAS Ctlgrs773586510
Max Magnitude0
ClinVar
Risk rs773586510(T;T)
Alt rs773586510(T;T)
Reference rs773586510(G;G)
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.128623228G>T
CLNSRC
CLNACC RCV000201722.1,