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rs387906950

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906950(A;G)
Make rs387906950(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position120739141
GeneACADS
is asnp
is mentioned by
dbSNPrs387906950
ebirs387906950
HLIrs387906950
Exacrs387906950
Varsomers387906950
Maprs387906950
PheGenIrs387906950
hapmaprs387906950
1000 genomesrs387906950
hgdprs387906950
ensemblrs387906950
gopubmedrs387906950
geneviewrs387906950
scholarrs387906950
googlers387906950
pharmgkbrs387906950
gwascentralrs387906950
openSNPrs387906950
23andMers387906950
23andMe allrs387906950
SNP Nexus

SNPshotrs387906950
SNPdbers387906950
MSV3drs387906950
GWAS Ctlgrs387906950
Max Magnitude0
ClinVar
Risk rs387906950(G;G)
Alt rs387906950(G;G)
Reference rs387906950(A;A)
Significance Other
Disease Deficiency of butyryl-CoA dehydrogenase
Variation info
Gene ACADS
CLNDBN Deficiency of butyryl-CoA dehydrogenase
Reversed 0
HGVS NC_000012.11:g.121176944A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023586.4,