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rs387906951

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906951(A;A)
Make rs387906951(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position120737098
GeneACADS
is asnp
is mentioned by
dbSNPrs387906951
ebirs387906951
HLIrs387906951
Exacrs387906951
Varsomers387906951
Maprs387906951
PheGenIrs387906951
hapmaprs387906951
1000 genomesrs387906951
hgdprs387906951
ensemblrs387906951
gopubmedrs387906951
geneviewrs387906951
scholarrs387906951
googlers387906951
pharmgkbrs387906951
gwascentralrs387906951
openSNPrs387906951
23andMers387906951
23andMe allrs387906951
SNP Nexus

SNPshotrs387906951
SNPdbers387906951
MSV3drs387906951
GWAS Ctlgrs387906951
Max Magnitude0
ClinVar
Risk rs387906951(A;A)
Alt rs387906951(A;A)
Reference rs387906951(G;G)
Significance Pathogenic
Disease Deficiency of butyryl-CoA dehydrogenase
Variation info
Gene ACADS
CLNDBN Deficiency of butyryl-CoA dehydrogenase
Reversed 0
HGVS NC_000012.11:g.121174901G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023587.2,