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rs113690956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113690956(G;T)
Make rs113690956(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position7223238
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs113690956
ebirs113690956
HLIrs113690956
Exacrs113690956
Varsomers113690956
Maprs113690956
PheGenIrs113690956
hapmaprs113690956
1000 genomesrs113690956
hgdprs113690956
ensemblrs113690956
gopubmedrs113690956
geneviewrs113690956
scholarrs113690956
googlers113690956
pharmgkbrs113690956
gwascentralrs113690956
openSNPrs113690956
23andMers113690956
23andMe allrs113690956
SNP Nexus

SNPshotrs113690956
SNPdbers113690956
MSV3drs113690956
GWAS Ctlgrs113690956
Max Magnitude0
ClinVar
Risk rs113690956(A,T;A,T)
Alt rs113690956(A,T;A,T)
Reference rs113690956(G;G)
Significance Other
Disease Very long chain acyl-CoA dehydrogenase deficiency
Variation info
Gene ACADVL MIR324
CLNDBN Very long chain acyl-CoA dehydrogenase deficiency
Reversed 0
HGVS NC_000017.10:g.7126557G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001689.3,