rs786204424
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs786204424(-;-) |
Make rs786204424(-;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 75733629 |
Gene | ACADM |
is a | snp |
is | mentioned by |
dbSNP | rs786204424 |
dbSNP (classic) | rs786204424 |
ClinGen | rs786204424 |
ebi | rs786204424 |
HLI | rs786204424 |
Exac | rs786204424 |
Gnomad | rs786204424 |
Varsome | rs786204424 |
LitVar | rs786204424 |
Map | rs786204424 |
PheGenI | rs786204424 |
Biobank | rs786204424 |
1000 genomes | rs786204424 |
hgdp | rs786204424 |
ensembl | rs786204424 |
geneview | rs786204424 |
scholar | rs786204424 |
rs786204424 | |
pharmgkb | rs786204424 |
gwascentral | rs786204424 |
openSNP | rs786204424 |
23andMe | rs786204424 |
SNPshot | rs786204424 |
SNPdbe | rs786204424 |
MSV3d | rs786204424 |
GWAS Ctlg | rs786204424 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786204424(-;-) |
Alt | rs786204424(-;-) |
Reference | Rs786204424(G;G) |
Significance | Probable-Pathogenic |
Disease | Medium-chain acyl-coenzyme A dehydrogenase deficiency not specified |
Variation | info |
Gene | ACADM |
CLNDBN | Medium-chain acyl-coenzyme A dehydrogenase deficiency not specified |
Reversed | 0 |
HGVS | NC_000001.10:g.76199314delG |
CLNSRC | Counsyl |
CLNACC | RCV000169015.1, RCV000383616.1, |