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rs370266841

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370266841(A;A)
Make rs370266841(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position128908215
GeneACAD9
is asnp
is mentioned by
dbSNPrs370266841
ebirs370266841
HLIrs370266841
Exacrs370266841
Varsomers370266841
Maprs370266841
PheGenIrs370266841
hapmaprs370266841
1000 genomesrs370266841
hgdprs370266841
ensemblrs370266841
gopubmedrs370266841
geneviewrs370266841
scholarrs370266841
googlers370266841
pharmgkbrs370266841
gwascentralrs370266841
openSNPrs370266841
23andMers370266841
23andMe allrs370266841
SNP Nexus

SNPshotrs370266841
SNPdbers370266841
MSV3drs370266841
GWAS Ctlgrs370266841
Max Magnitude0
ClinVar
Risk rs370266841(A;A)
Alt rs370266841(A;A)
Reference rs370266841(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACAD9
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.128627058G>A
CLNSRC
CLNACC RCV000195577.2,