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rs113994170

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs113994170(C;T)
Make rs113994170(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7224040
GeneACADVL
is asnp
is mentioned by
dbSNPrs113994170
ebirs113994170
HLIrs113994170
Exacrs113994170
Varsomers113994170
Maprs113994170
PheGenIrs113994170
hapmaprs113994170
1000 genomesrs113994170
hgdprs113994170
ensemblrs113994170
gopubmedrs113994170
geneviewrs113994170
scholarrs113994170
googlers113994170
pharmgkbrs113994170
gwascentralrs113994170
openSNPrs113994170
23andMers113994170
23andMe allrs113994170
SNP Nexus

SNPshotrs113994170
SNPdbers113994170
MSV3drs113994170
GWAS Ctlgrs113994170
Max Magnitude0
ClinVar
Risk rs113994170(T;T)
Alt rs113994170(T;T)
Reference rs113994170(C;C)
Significance Other
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.7127359C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020073.3,


OMIM201475
Desc
Variant
Relatedalso