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rs754359356

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs754359356(A;A)
Make rs754359356(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position75740069
GeneACADM
is asnp
is mentioned by
dbSNPrs754359356
dbSNP (classic)rs754359356
ClinGenrs754359356
ebirs754359356
HLIrs754359356
Exacrs754359356
Gnomadrs754359356
Varsomers754359356
LitVarrs754359356
Maprs754359356
PheGenIrs754359356
Biobankrs754359356
1000 genomesrs754359356
hgdprs754359356
ensemblrs754359356
geneviewrs754359356
scholarrs754359356
googlers754359356
pharmgkbrs754359356
gwascentralrs754359356
openSNPrs754359356
23andMers754359356
23andMe allrs754359356
SNPshotrs754359356
SNPdbers754359356
MSV3drs754359356
GWAS Ctlgrs754359356
Max Magnitude0
ClinVar
Risk rs754359356(A;A) rs754359356(C;C)
Alt rs754359356(A;A) rs754359356(C;C)
Reference Rs754359356(T;T)
Significance Probable-Pathogenic
Disease not specified Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided
Variation info
Gene ACADM
CLNDBN not specified Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided
Reversed 0
HGVS NC_000001.10:g.76205754T>A
CLNSRC
CLNACC RCV000179694.1, RCV000211498.1, RCV000421950.1,