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rs863223875

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223875(C;C)
Make rs863223875(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128904090
GeneACAD9
is asnp
is mentioned by
dbSNPrs863223875
ebirs863223875
HLIrs863223875
Exacrs863223875
Varsomers863223875
Maprs863223875
PheGenIrs863223875
hapmaprs863223875
1000 genomesrs863223875
hgdprs863223875
ensemblrs863223875
gopubmedrs863223875
geneviewrs863223875
scholarrs863223875
googlers863223875
pharmgkbrs863223875
gwascentralrs863223875
openSNPrs863223875
23andMers863223875
23andMe allrs863223875
SNP Nexus

SNPshotrs863223875
SNPdbers863223875
MSV3drs863223875
GWAS Ctlgrs863223875
Max Magnitude0
ClinVar
Risk rs863223875(C;C)
Alt rs863223875(C;C)
Reference rs863223875(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACAD9
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.128622933G>C
CLNSRC
CLNACC RCV000200760.1,