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

rs387906308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
(GGA;GGA) 0 common in clinvar
Make rs387906308(-;-)
Make rs387906308(-;GAG)
ReferenceGRCh38 38.1/141
Chromosome12
Position120737085
GeneACADS
is asnp
is mentioned by
dbSNPrs387906308
ebirs387906308
HLIrs387906308
Exacrs387906308
Varsomers387906308
Maprs387906308
PheGenIrs387906308
hapmaprs387906308
1000 genomesrs387906308
hgdprs387906308
ensemblrs387906308
gopubmedrs387906308
geneviewrs387906308
scholarrs387906308
googlers387906308
pharmgkbrs387906308
gwascentralrs387906308
openSNPrs387906308
23andMers387906308
23andMe allrs387906308
SNP Nexus

SNPshotrs387906308
SNPdbers387906308
MSV3drs387906308
GWAS Ctlgrs387906308
Max Magnitude0
ClinVar
Risk rs387906308(;)
Alt rs387906308(;)
Reference rs387906308(GGA;GGA)
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.121174888_121174890delGAG
CLNSRC OMIM Allelic Variant
CLNACC RCV000004037.2, RCV000185702.1,