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rs753711253

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs753711253(C;T)
Make rs753711253(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128899449
GeneACAD9
is asnp
is mentioned by
dbSNPrs753711253
ebirs753711253
HLIrs753711253
Exacrs753711253
Varsomers753711253
Maprs753711253
PheGenIrs753711253
hapmaprs753711253
1000 genomesrs753711253
hgdprs753711253
ensemblrs753711253
gopubmedrs753711253
geneviewrs753711253
scholarrs753711253
googlers753711253
pharmgkbrs753711253
gwascentralrs753711253
openSNPrs753711253
23andMers753711253
23andMe allrs753711253
SNP Nexus

SNPshotrs753711253
SNPdbers753711253
MSV3drs753711253
GWAS Ctlgrs753711253
Max Magnitude0
ClinVar
Risk rs753711253(T;T)
Alt rs753711253(T;T)
Reference rs753711253(C;C)
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.128618292C>T
CLNSRC
CLNACC RCV000201531.1,