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rs368949613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368949613(C;T)
Make rs368949613(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position128906220
GeneACAD9
is asnp
is mentioned by
dbSNPrs368949613
ebirs368949613
HLIrs368949613
Exacrs368949613
Varsomers368949613
Maprs368949613
PheGenIrs368949613
hapmaprs368949613
1000 genomesrs368949613
hgdprs368949613
ensemblrs368949613
gopubmedrs368949613
geneviewrs368949613
scholarrs368949613
googlers368949613
pharmgkbrs368949613
gwascentralrs368949613
openSNPrs368949613
23andMers368949613
23andMe allrs368949613
SNP Nexus

SNPshotrs368949613
SNPdbers368949613
MSV3drs368949613
GWAS Ctlgrs368949613
Max Magnitude0
ClinVar
Risk rs368949613(T;T)
Alt rs368949613(T;T)
Reference rs368949613(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.128625063C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023865.2, RCV000201722.1,