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

rs786204566

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786204566(-;-)
Make rs786204566(-;T)
Make rs786204566(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position75732880
GeneACADM
is asnp
is mentioned by
dbSNPrs786204566
ebirs786204566
HLIrs786204566
Exacrs786204566
Varsomers786204566
Maprs786204566
PheGenIrs786204566
hapmaprs786204566
1000 genomesrs786204566
hgdprs786204566
ensemblrs786204566
gopubmedrs786204566
geneviewrs786204566
scholarrs786204566
googlers786204566
pharmgkbrs786204566
gwascentralrs786204566
openSNPrs786204566
23andMers786204566
23andMe allrs786204566
SNP Nexus

SNPshotrs786204566
SNPdbers786204566
MSV3drs786204566
GWAS Ctlgrs786204566
Max Magnitude0
ClinVar
Risk rs786204566(T;T)
Alt rs786204566(T;T)
Reference rs786204566(;)
Significance Pathogenic
Disease Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided
Variation info
Gene ACADM
CLNDBN Medium-chain acyl-coenzyme A dehydrogenase deficiency not provided
Reversed 0
HGVS NC_000001.10:g.76198565dupT
CLNSRC Counsyl
CLNACC RCV000169305.1, RCV000185677.2,