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rs121908003

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908003(C;T)
Make rs121908003(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120727115
GeneACADS
is asnp
is mentioned by
dbSNPrs121908003
ebirs121908003
HLIrs121908003
Exacrs121908003
Varsomers121908003
Maprs121908003
PheGenIrs121908003
hapmaprs121908003
1000 genomesrs121908003
hgdprs121908003
ensemblrs121908003
gopubmedrs121908003
geneviewrs121908003
scholarrs121908003
googlers121908003
pharmgkbrs121908003
gwascentralrs121908003
openSNPrs121908003
23andMers121908003
23andMe allrs121908003
SNP Nexus

SNPshotrs121908003
SNPdbers121908003
MSV3drs121908003
GWAS Ctlgrs121908003
Max Magnitude0
OMIM606885
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908003(T;T)
Alt rs121908003(T;T)
Reference rs121908003(C;C)
Significance Other
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.121164918C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004029.4, RCV000185706.2,