Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908006

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908006(C;T)
Make rs121908006(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120738859
GeneACADS
is asnp
is mentioned by
dbSNPrs121908006
ebirs121908006
HLIrs121908006
Exacrs121908006
Varsomers121908006
Maprs121908006
PheGenIrs121908006
hapmaprs121908006
1000 genomesrs121908006
hgdprs121908006
ensemblrs121908006
gopubmedrs121908006
geneviewrs121908006
scholarrs121908006
googlers121908006
pharmgkbrs121908006
gwascentralrs121908006
openSNPrs121908006
23andMers121908006
23andMe allrs121908006
SNP Nexus

SNPshotrs121908006
SNPdbers121908006
MSV3drs121908006
GWAS Ctlgrs121908006
Max Magnitude0
OMIM606885
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121908006(T;T)
Alt rs121908006(T;T)
Reference rs121908006(C;C)
Significance Pathogenic
Disease Deficiency of butyryl-CoA dehydrogenase not provided
Variation info
Gene ACADS
CLNDBN Deficiency of butyryl-CoA dehydrogenase not provided
Reversed 0
HGVS NC_000012.11:g.121176662C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004039.2, RCV000185689.2,