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rs115532916

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs115532916(A;A)
Make rs115532916(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position128904079
GeneACAD9
is asnp
is mentioned by
dbSNPrs115532916
ebirs115532916
HLIrs115532916
Exacrs115532916
Varsomers115532916
Maprs115532916
PheGenIrs115532916
hapmaprs115532916
1000 genomesrs115532916
hgdprs115532916
ensemblrs115532916
gopubmedrs115532916
geneviewrs115532916
scholarrs115532916
googlers115532916
pharmgkbrs115532916
gwascentralrs115532916
openSNPrs115532916
23andMers115532916
23andMe allrs115532916
SNP Nexus

SNPshotrs115532916
SNPdbers115532916
MSV3drs115532916
GWAS Ctlgrs115532916
GMAF0.0101
Max Magnitude0
ClinVar
Risk rs115532916(A,C;A,C)
Alt rs115532916(A,C;A,C)
Reference rs115532916(G;G)
Significance Pathogenic
Disease not specified Acyl-CoA dehydrogenase family not provided
Variation info
Gene ACAD9
CLNDBN not specified Acyl-CoA dehydrogenase family, member 9, deficiency of not provided
Reversed 0
HGVS NC_000003.11:g.128622922G>A; NC_000003.11:g.128622922G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000123467.1, RCV000201693.1, RCV000023868.2, RCV000198883.2,