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rs1057518752

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518752(C;G)
Make rs1057518752(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position128910144
GeneACAD9, KIAA1257
is asnp
is mentioned by
dbSNPrs1057518752
dbSNP (old)rs1057518752
ClinGenrs1057518752
ebirs1057518752
HLIrs1057518752
Exacrs1057518752
Gnomadrs1057518752
Varsomers1057518752
Maprs1057518752
PheGenIrs1057518752
Biobankrs1057518752
1000 genomesrs1057518752
hgdprs1057518752
ensemblrs1057518752
gopubmedrs1057518752
geneviewrs1057518752
scholarrs1057518752
googlers1057518752
pharmgkbrs1057518752
gwascentralrs1057518752
openSNPrs1057518752
23andMers1057518752
23andMe allrs1057518752
SNPshotrs1057518752
SNPdbers1057518752
MSV3drs1057518752
GWAS Ctlgrs1057518752
Max Magnitude0
ClinVar
Risk rs1057518752(G;G)
Alt rs1057518752(G;G)
Reference Rs1057518752(C;C)
Significance Pathogenic
Disease Acyl-CoA dehydrogenase family
Variation info
Gene LOC100132731 ACAD9
CLNDBN Acyl-CoA dehydrogenase family, member 9, deficiency of
Reversed 0
HGVS NC_000003.11:g.128628987C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000412667.1,