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rs745844469

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs745844469(A;C)
Make rs745844469(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position75740014
GeneACADM
is asnp
is mentioned by
dbSNPrs745844469
dbSNP (classic)rs745844469
ClinGenrs745844469
ebirs745844469
HLIrs745844469
Exacrs745844469
Gnomadrs745844469
Varsomers745844469
LitVarrs745844469
Maprs745844469
PheGenIrs745844469
Biobankrs745844469
1000 genomesrs745844469
hgdprs745844469
ensemblrs745844469
geneviewrs745844469
scholarrs745844469
googlers745844469
pharmgkbrs745844469
gwascentralrs745844469
openSNPrs745844469
23andMers745844469
23andMe allrs745844469
SNPshotrs745844469
SNPdbers745844469
MSV3drs745844469
GWAS Ctlgrs745844469
Max Magnitude0
ClinVar
Risk rs745844469(C;C)
Alt rs745844469(C;C)
Reference Rs745844469(A;A)
Significance Probable-Pathogenic
Disease Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided
Variation info
Gene ACADM
CLNDBN Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided
Reversed 0
HGVS NC_000001.10:g.76205699A>C
CLNSRC
CLNACC RCV000211496.1, RCV000439614.1,