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rs770127110

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770127110(A;A)
Make rs770127110(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128910052
GeneACAD9, KIAA1257
is asnp
is mentioned by
dbSNPrs770127110
ebirs770127110
HLIrs770127110
Exacrs770127110
Varsomers770127110
Maprs770127110
PheGenIrs770127110
hapmaprs770127110
1000 genomesrs770127110
hgdprs770127110
ensemblrs770127110
gopubmedrs770127110
geneviewrs770127110
scholarrs770127110
googlers770127110
pharmgkbrs770127110
gwascentralrs770127110
openSNPrs770127110
23andMers770127110
23andMe allrs770127110
SNP Nexus

SNPshotrs770127110
SNPdbers770127110
MSV3drs770127110
GWAS Ctlgrs770127110
Max Magnitude0
ClinVar
Risk rs770127110(A;A)
Alt rs770127110(A;A)
Reference rs770127110(G;G)
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.128628895G>A
CLNSRC
CLNACC RCV000201693.1,