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rs398124269

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398124269(-;-)
Make rs398124269(-;CT)
Make rs398124269(CT;CT)
ReferenceGRCh38 38.1/141
Chromosome11
Position134258582
GeneACAD8
is asnp
is mentioned by
dbSNPrs398124269
ebirs398124269
HLIrs398124269
Exacrs398124269
Varsomers398124269
Maprs398124269
PheGenIrs398124269
hapmaprs398124269
1000 genomesrs398124269
hgdprs398124269
ensemblrs398124269
gopubmedrs398124269
geneviewrs398124269
scholarrs398124269
googlers398124269
pharmgkbrs398124269
gwascentralrs398124269
openSNPrs398124269
23andMers398124269
23andMe allrs398124269
SNP Nexus

SNPshotrs398124269
SNPdbers398124269
MSV3drs398124269
GWAS Ctlgrs398124269
Max Magnitude0
ClinVar
Risk rs398124269(CT;CT)
Alt rs398124269(CT;CT)
Reference rs398124269(;)
Significance Pathogenic
Disease not provided
Variation info
Gene ACAD8
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.134128475_134128476dupCT
CLNSRC ClinVar
CLNACC RCV000081619.4,