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rs398123082

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123082(-;-)
Make rs398123082(-;G)
Make rs398123082(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7224024
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs398123082
ebirs398123082
HLIrs398123082
Exacrs398123082
Varsomers398123082
Maprs398123082
PheGenIrs398123082
hapmaprs398123082
1000 genomesrs398123082
hgdprs398123082
ensemblrs398123082
gopubmedrs398123082
geneviewrs398123082
scholarrs398123082
googlers398123082
pharmgkbrs398123082
gwascentralrs398123082
openSNPrs398123082
23andMers398123082
23andMe allrs398123082
SNP Nexus

SNPshotrs398123082
SNPdbers398123082
MSV3drs398123082
GWAS Ctlgrs398123082
Max Magnitude0
ClinVar
Risk rs398123082(G;G)
Alt rs398123082(G;G)
Reference rs398123082(;)
Significance Pathogenic
Disease not provided Very long chain acyl-CoA dehydrogenase deficiency
Variation info
Gene MIR324 ACADVL
CLNDBN not provided Very long chain acyl-CoA dehydrogenase deficiency
Reversed 0
HGVS NC_000017.10:g.7127343dupG
CLNSRC ClinVar
CLNACC RCV000077905.3, RCV000174651.1,