rs6868223
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6868223(A;A) |
Make rs6868223(A;G) |
Make rs6868223(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 33636489 |
Gene | ADAMTS12 |
is a | snp |
is | mentioned by |
dbSNP | rs6868223 |
dbSNP (classic) | rs6868223 |
ClinGen | rs6868223 |
ebi | rs6868223 |
HLI | rs6868223 |
Exac | rs6868223 |
Gnomad | rs6868223 |
Varsome | rs6868223 |
LitVar | rs6868223 |
Map | rs6868223 |
PheGenI | rs6868223 |
Biobank | rs6868223 |
1000 genomes | rs6868223 |
hgdp | rs6868223 |
ensembl | rs6868223 |
geneview | rs6868223 |
scholar | rs6868223 |
rs6868223 | |
pharmgkb | rs6868223 |
gwascentral | rs6868223 |
openSNP | rs6868223 |
23andMe | rs6868223 |
SNPshot | rs6868223 |
SNPdbe | rs6868223 |
MSV3d | rs6868223 |
GWAS Ctlg | rs6868223 |
GMAF | 0.4591 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20400778] |
Trait | Mortality among heart failure patients |
Title | Genomic Variation Associated with Mortality among Adults of European and African Ancestry with Heart Failure: The CHARGE Consortium |
Risk Allele | A |
P-val | 0.000002 |
Odds Ratio | 1.58 [0.98-2.56] |