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rs398123083

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123083(A;A)
Make rs398123083(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7224041
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs398123083
ebirs398123083
HLIrs398123083
Exacrs398123083
Varsomers398123083
Maprs398123083
PheGenIrs398123083
hapmaprs398123083
1000 genomesrs398123083
hgdprs398123083
ensemblrs398123083
gopubmedrs398123083
geneviewrs398123083
scholarrs398123083
googlers398123083
pharmgkbrs398123083
gwascentralrs398123083
openSNPrs398123083
23andMers398123083
23andMe allrs398123083
SNP Nexus

SNPshotrs398123083
SNPdbers398123083
MSV3drs398123083
GWAS Ctlgrs398123083
Max Magnitude0
ClinVar
Risk rs398123083(A;A)
Alt rs398123083(A;A)
Reference rs398123083(G;G)
Significance Other
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.7127360G>A
CLNSRC HGMD
CLNACC RCV000077906.3, RCV000169627.2,