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rs398123094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs398123094(-;-)
Make rs398123094(-;AGA)
ReferenceGRCh38 38.1/141
Chromosome17
Position7222684
GeneACADVL
is asnp
is mentioned by
dbSNPrs398123094
ebirs398123094
HLIrs398123094
Exacrs398123094
Varsomers398123094
Maprs398123094
PheGenIrs398123094
hapmaprs398123094
1000 genomesrs398123094
hgdprs398123094
ensemblrs398123094
gopubmedrs398123094
geneviewrs398123094
scholarrs398123094
googlers398123094
pharmgkbrs398123094
gwascentralrs398123094
openSNPrs398123094
23andMers398123094
23andMe allrs398123094
SNP Nexus

SNPshotrs398123094
SNPdbers398123094
MSV3drs398123094
GWAS Ctlgrs398123094
Max Magnitude0
ClinVar
Risk rs398123094(;)
Alt rs398123094(;)
Reference rs398123094(AGA;AGA)
Significance Other
Disease Very long chain acyl-CoA dehydrogenase deficiency not provided
Variation info
Gene ACADVL
CLNDBN Very long chain acyl-CoA dehydrogenase deficiency not provided
Reversed 0
HGVS NC_000017.10:g.7126003_7126005delAGA
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000001694.5, RCV000077926.3,