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rs781156571

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781156571(A;A)
Make rs781156571(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128908204
GeneACAD9
is asnp
is mentioned by
dbSNPrs781156571
ebirs781156571
HLIrs781156571
Exacrs781156571
Varsomers781156571
Maprs781156571
PheGenIrs781156571
hapmaprs781156571
1000 genomesrs781156571
hgdprs781156571
ensemblrs781156571
gopubmedrs781156571
geneviewrs781156571
scholarrs781156571
googlers781156571
pharmgkbrs781156571
gwascentralrs781156571
openSNPrs781156571
23andMers781156571
23andMe allrs781156571
SNP Nexus

SNPshotrs781156571
SNPdbers781156571
MSV3drs781156571
GWAS Ctlgrs781156571
Max Magnitude0
ClinVar
Risk rs781156571(A;A)
Alt rs781156571(A;A)
Reference rs781156571(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.128627047G>A
CLNSRC
CLNACC RCV000201557.1,