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rs794727113

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727113(C;T)
Make rs794727113(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7223992
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs794727113
ebirs794727113
HLIrs794727113
Exacrs794727113
Varsomers794727113
Maprs794727113
PheGenIrs794727113
hapmaprs794727113
1000 genomesrs794727113
hgdprs794727113
ensemblrs794727113
gopubmedrs794727113
geneviewrs794727113
scholarrs794727113
googlers794727113
pharmgkbrs794727113
gwascentralrs794727113
openSNPrs794727113
23andMers794727113
23andMe allrs794727113
SNP Nexus

SNPshotrs794727113
SNPdbers794727113
MSV3drs794727113
GWAS Ctlgrs794727113
Max Magnitude0
ClinVar
Risk rs794727113(T;T)
Alt rs794727113(T;T)
Reference rs794727113(C;C)
Significance Pathogenic
Disease Very long chain acyl-CoA dehydrogenase deficiency
Variation info
Gene MIR324 ACADVL
CLNDBN Very long chain acyl-CoA dehydrogenase deficiency
Reversed 0
HGVS NC_000017.10:g.7127311C>T
CLNSRC
CLNACC RCV000174654.1,