Have questions? Visit https://www.reddit.com/r/SNPedia

rs113994171

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113994171(A;A)
Make rs113994171(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position7224636
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs113994171
ebirs113994171
HLIrs113994171
Exacrs113994171
Varsomers113994171
Maprs113994171
PheGenIrs113994171
hapmaprs113994171
1000 genomesrs113994171
hgdprs113994171
ensemblrs113994171
gopubmedrs113994171
geneviewrs113994171
scholarrs113994171
googlers113994171
pharmgkbrs113994171
gwascentralrs113994171
openSNPrs113994171
23andMers113994171
23andMe allrs113994171
SNP Nexus

SNPshotrs113994171
SNPdbers113994171
MSV3drs113994171
GWAS Ctlgrs113994171
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs113994171(A;A)
Alt rs113994171(A;A)
Reference rs113994171(G;G)
Significance Other
Disease Very long chain acyl-CoA dehydrogenase deficiency not provided
Variation info
Gene MIR324 ACADVL
CLNDBN Very long chain acyl-CoA dehydrogenase deficiency not provided
Reversed 0
HGVS NC_000017.10:g.7127955G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000031857.3, RCV000185730.1,