rs796051899
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs796051899(A;A) |
Make rs796051899(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 75733558 |
Gene | ACADM |
is a | snp |
is | mentioned by |
dbSNP | rs796051899 |
dbSNP (classic) | rs796051899 |
ClinGen | rs796051899 |
ebi | rs796051899 |
HLI | rs796051899 |
Exac | rs796051899 |
Gnomad | rs796051899 |
Varsome | rs796051899 |
LitVar | rs796051899 |
Map | rs796051899 |
PheGenI | rs796051899 |
Biobank | rs796051899 |
1000 genomes | rs796051899 |
hgdp | rs796051899 |
ensembl | rs796051899 |
geneview | rs796051899 |
scholar | rs796051899 |
rs796051899 | |
pharmgkb | rs796051899 |
gwascentral | rs796051899 |
openSNP | rs796051899 |
23andMe | rs796051899 |
SNPshot | rs796051899 |
SNPdbe | rs796051899 |
MSV3d | rs796051899 |
GWAS Ctlg | rs796051899 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796051899(A;A) |
Alt | rs796051899(A;A) |
Reference | Rs796051899(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACADM |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.76199243G>A |
CLNSRC | |
CLNACC | RCV000185672.1, |