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rs773949927

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs773949927(A;T)
Make rs773949927(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128879692
GeneACAD9
is asnp
is mentioned by
dbSNPrs773949927
ebirs773949927
HLIrs773949927
Exacrs773949927
Varsomers773949927
Maprs773949927
PheGenIrs773949927
hapmaprs773949927
1000 genomesrs773949927
hgdprs773949927
ensemblrs773949927
gopubmedrs773949927
geneviewrs773949927
scholarrs773949927
googlers773949927
pharmgkbrs773949927
gwascentralrs773949927
openSNPrs773949927
23andMers773949927
23andMe allrs773949927
SNP Nexus

SNPshotrs773949927
SNPdbers773949927
MSV3drs773949927
GWAS Ctlgrs773949927
Max Magnitude0
ClinVar
Risk rs773949927(T;T)
Alt rs773949927(T;T)
Reference rs773949927(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.128598535A>G
CLNSRC
CLNACC RCV000201531.1,