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rs747610156

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs747610156(-;-)
Make rs747610156(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75761160
GeneACADM
is asnp
is mentioned by
dbSNPrs747610156
ebirs747610156
HLIrs747610156
Exacrs747610156
Varsomers747610156
Maprs747610156
PheGenIrs747610156
hapmaprs747610156
1000 genomesrs747610156
hgdprs747610156
ensemblrs747610156
gopubmedrs747610156
geneviewrs747610156
scholarrs747610156
googlers747610156
pharmgkbrs747610156
gwascentralrs747610156
openSNPrs747610156
23andMers747610156
23andMe allrs747610156
SNP Nexus

SNPshotrs747610156
SNPdbers747610156
MSV3drs747610156
GWAS Ctlgrs747610156
Max Magnitude0
ClinVar
Risk rs747610156(;)
Alt rs747610156(;)
Reference rs747610156(G;G)
Significance Pathogenic
Disease Medium-chain acyl-coenzyme A dehydrogenase deficiency
Variation info
Gene ACADM
CLNDBN Medium-chain acyl-coenzyme A dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.76226845delG
CLNSRC
CLNACC RCV000211482.1,