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rs863223876

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223876(A;G)
Make rs863223876(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128906224
GeneACAD9
is asnp
is mentioned by
dbSNPrs863223876
ebirs863223876
HLIrs863223876
Exacrs863223876
Varsomers863223876
Maprs863223876
PheGenIrs863223876
hapmaprs863223876
1000 genomesrs863223876
hgdprs863223876
ensemblrs863223876
gopubmedrs863223876
geneviewrs863223876
scholarrs863223876
googlers863223876
pharmgkbrs863223876
gwascentralrs863223876
openSNPrs863223876
23andMers863223876
23andMe allrs863223876
SNP Nexus

SNPshotrs863223876
SNPdbers863223876
MSV3drs863223876
GWAS Ctlgrs863223876
Max Magnitude0
ClinVar
Risk rs863223876(G;G)
Alt rs863223876(G;G)
Reference rs863223876(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACAD9
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.128625067A>G
CLNSRC
CLNACC RCV000195437.1,