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rs786204691

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs786204691(-;-)
Make rs786204691(-;GA)
Make rs786204691(GA;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position120738337
GeneACADS
is asnp
is mentioned by
dbSNPrs786204691
ebirs786204691
HLIrs786204691
Exacrs786204691
Varsomers786204691
Maprs786204691
PheGenIrs786204691
hapmaprs786204691
1000 genomesrs786204691
hgdprs786204691
ensemblrs786204691
gopubmedrs786204691
geneviewrs786204691
scholarrs786204691
googlers786204691
pharmgkbrs786204691
gwascentralrs786204691
openSNPrs786204691
23andMers786204691
23andMe allrs786204691
SNP Nexus

SNPshotrs786204691
SNPdbers786204691
MSV3drs786204691
GWAS Ctlgrs786204691
Max Magnitude0
ClinVar
Risk rs786204691(;)
Alt rs786204691(;)
Reference rs786204691(AG;AG)
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.121176140_121176141delGA
CLNSRC Counsyl
CLNACC RCV000169499.1, RCV000185707.1,