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rs727503794

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503794(A;A)
Make rs727503794(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7224244
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs727503794
ebirs727503794
HLIrs727503794
Exacrs727503794
Varsomers727503794
Maprs727503794
PheGenIrs727503794
hapmaprs727503794
1000 genomesrs727503794
hgdprs727503794
ensemblrs727503794
gopubmedrs727503794
geneviewrs727503794
scholarrs727503794
googlers727503794
pharmgkbrs727503794
gwascentralrs727503794
openSNPrs727503794
23andMers727503794
23andMe allrs727503794
SNP Nexus

SNPshotrs727503794
SNPdbers727503794
MSV3drs727503794
GWAS Ctlgrs727503794
Max Magnitude0
ClinVar
Risk rs727503794(A;A)
Alt rs727503794(A;A)
Reference rs727503794(G;G)
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.7127563G>A
CLNSRC
CLNACC RCV000152740.3,