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rs779379787

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779379787(A;A)
Make rs779379787(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128908189
GeneACAD9
is asnp
is mentioned by
dbSNPrs779379787
ebirs779379787
HLIrs779379787
Exacrs779379787
Varsomers779379787
Maprs779379787
PheGenIrs779379787
hapmaprs779379787
1000 genomesrs779379787
hgdprs779379787
ensemblrs779379787
gopubmedrs779379787
geneviewrs779379787
scholarrs779379787
googlers779379787
pharmgkbrs779379787
gwascentralrs779379787
openSNPrs779379787
23andMers779379787
23andMe allrs779379787
SNP Nexus

SNPshotrs779379787
SNPdbers779379787
MSV3drs779379787
GWAS Ctlgrs779379787
Max Magnitude0
ClinVar
Risk rs779379787(A;A)
Alt rs779379787(A;A)
Reference rs779379787(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACAD9
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.128627032C>T
CLNSRC
CLNACC RCV000197980.1,