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rs200771970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200771970(A;A)
Make rs200771970(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position7224243
GeneACADVL, MIR324
is asnp
is mentioned by
dbSNPrs200771970
dbSNP (old)rs200771970
ClinGenrs200771970
ebirs200771970
HLIrs200771970
Exacrs200771970
Gnomadrs200771970
Varsomers200771970
Maprs200771970
PheGenIrs200771970
Biobankrs200771970
1000 genomesrs200771970
hgdprs200771970
ensemblrs200771970
gopubmedrs200771970
geneviewrs200771970
scholarrs200771970
googlers200771970
pharmgkbrs200771970
gwascentralrs200771970
openSNPrs200771970
23andMers200771970
23andMe allrs200771970
SNP Nexus

SNPshotrs200771970
SNPdbers200771970
MSV3drs200771970
GWAS Ctlgrs200771970
Max Magnitude0
ClinVar
Risk rs200771970(A;A)
Alt rs200771970(A;A)
Reference Rs200771970(G;G)
Significance Probable-Pathogenic
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.7127562G>A
CLNSRC
CLNACC RCV000410771.1,