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rs778906552

From SNPedia

Orientationplus
Stabilizedplus
Make rs778906552(A;A)
Make rs778906552(A;G)
Make rs778906552(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75734846
GeneACADM
is asnp
is mentioned by
dbSNPrs778906552
dbSNP (old)rs778906552
ClinGenrs778906552
ebirs778906552
HLIrs778906552
Exacrs778906552
Gnomadrs778906552
Varsomers778906552
Maprs778906552
PheGenIrs778906552
Biobankrs778906552
1000 genomesrs778906552
hgdprs778906552
ensemblrs778906552
gopubmedrs778906552
geneviewrs778906552
scholarrs778906552
googlers778906552
pharmgkbrs778906552
gwascentralrs778906552
openSNPrs778906552
23andMers778906552
23andMe allrs778906552
SNP Nexus

SNPshotrs778906552
SNPdbers778906552
MSV3drs778906552
GWAS Ctlgrs778906552
Max Magnitude
ClinVar
Risk rs778906552(A;A)
Alt rs778906552(A;A)
Reference rs778906552(G;G)
Significance Other
Disease not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency
Variation info
Gene ACADM
CLNDBN not provided Medium-chain acyl-coenzyme A dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.76200531G>A
CLNSRC
CLNACC RCV000179231.4, RCV000211501.2,