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rs778558550

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs778558550(A;A)
Make rs778558550(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128910763
GeneACAD9, KIAA1257
is asnp
is mentioned by
dbSNPrs778558550
ebirs778558550
HLIrs778558550
Exacrs778558550
Varsomers778558550
Maprs778558550
PheGenIrs778558550
hapmaprs778558550
1000 genomesrs778558550
hgdprs778558550
ensemblrs778558550
gopubmedrs778558550
geneviewrs778558550
scholarrs778558550
googlers778558550
pharmgkbrs778558550
gwascentralrs778558550
openSNPrs778558550
23andMers778558550
23andMe allrs778558550
SNP Nexus

SNPshotrs778558550
SNPdbers778558550
MSV3drs778558550
GWAS Ctlgrs778558550
Max Magnitude0
ClinVar
Risk rs778558550(A;A)
Alt rs778558550(A;A)
Reference rs778558550(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC100132731 ACAD9
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.128629606G>A
CLNSRC
CLNACC RCV000198124.1,