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rs796051896

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796051896(C;G)
Make rs796051896(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position75761188
GeneACADM
is asnp
is mentioned by
dbSNPrs796051896
ebirs796051896
HLIrs796051896
Exacrs796051896
Varsomers796051896
Maprs796051896
PheGenIrs796051896
hapmaprs796051896
1000 genomesrs796051896
hgdprs796051896
ensemblrs796051896
gopubmedrs796051896
geneviewrs796051896
scholarrs796051896
googlers796051896
pharmgkbrs796051896
gwascentralrs796051896
openSNPrs796051896
23andMers796051896
23andMe allrs796051896
SNP Nexus

SNPshotrs796051896
SNPdbers796051896
MSV3drs796051896
GWAS Ctlgrs796051896
Max Magnitude0
ClinVar
Risk rs796051896(G,T;G,T)
Alt rs796051896(G,T;G,T)
Reference rs796051896(C;C)
Significance Pathogenic
Disease not specified Medium-chain acyl-coenzyme A dehydrogenase deficiency
Variation info
Gene ACADM
CLNDBN not specified Medium-chain acyl-coenzyme A dehydrogenase deficiency
Reversed 0
HGVS NC_000001.10:g.76226873C>G; NC_000001.10:g.76226873C>T
CLNSRC
CLNACC RCV000185666.1, RCV000211507.1,