rs768884003
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs768884003(A;A) |
Make rs768884003(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 75749467 |
Gene | ACADM |
is a | snp |
is | mentioned by |
dbSNP | rs768884003 |
dbSNP (classic) | rs768884003 |
ClinGen | rs768884003 |
ebi | rs768884003 |
HLI | rs768884003 |
Exac | rs768884003 |
Gnomad | rs768884003 |
Varsome | rs768884003 |
LitVar | rs768884003 |
Map | rs768884003 |
PheGenI | rs768884003 |
Biobank | rs768884003 |
1000 genomes | rs768884003 |
hgdp | rs768884003 |
ensembl | rs768884003 |
geneview | rs768884003 |
scholar | rs768884003 |
rs768884003 | |
pharmgkb | rs768884003 |
gwascentral | rs768884003 |
openSNP | rs768884003 |
23andMe | rs768884003 |
SNPshot | rs768884003 |
SNPdbe | rs768884003 |
MSV3d | rs768884003 |
GWAS Ctlg | rs768884003 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768884003(A;A) |
Alt | rs768884003(A;A) |
Reference | Rs768884003(G;G) |
Significance | Probable-Pathogenic |
Disease | Medium-chain acyl-coenzyme A dehydrogenase deficiency |
Variation | info |
Gene | ACADM |
CLNDBN | Medium-chain acyl-coenzyme A dehydrogenase deficiency |
Reversed | 0 |
HGVS | NC_000001.10:g.76215152G>A |
CLNSRC | |
CLNACC | RCV000211500.1, |