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rs863223873

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223873(G;G)
Make rs863223873(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128896479
GeneACAD9
is asnp
is mentioned by
dbSNPrs863223873
ebirs863223873
HLIrs863223873
Exacrs863223873
Varsomers863223873
Maprs863223873
PheGenIrs863223873
hapmaprs863223873
1000 genomesrs863223873
hgdprs863223873
ensemblrs863223873
gopubmedrs863223873
geneviewrs863223873
scholarrs863223873
googlers863223873
pharmgkbrs863223873
gwascentralrs863223873
openSNPrs863223873
23andMers863223873
23andMe allrs863223873
SNP Nexus

SNPshotrs863223873
SNPdbers863223873
MSV3drs863223873
GWAS Ctlgrs863223873
Max Magnitude0
ClinVar
Risk rs863223873(G;G)
Alt rs863223873(G;G)
Reference rs863223873(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACAD9
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.128615322T>G
CLNSRC
CLNACC RCV000198768.1,