rs1448817
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1448817(A;A) |
Make rs1448817(A;G) |
Make rs1448817(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 110719897 |
is a | snp |
is | mentioned by |
dbSNP | rs1448817 |
dbSNP (classic) | rs1448817 |
ClinGen | rs1448817 |
ebi | rs1448817 |
HLI | rs1448817 |
Exac | rs1448817 |
Gnomad | rs1448817 |
Varsome | rs1448817 |
LitVar | rs1448817 |
Map | rs1448817 |
PheGenI | rs1448817 |
Biobank | rs1448817 |
1000 genomes | rs1448817 |
hgdp | rs1448817 |
ensembl | rs1448817 |
geneview | rs1448817 |
scholar | rs1448817 |
rs1448817 | |
pharmgkb | rs1448817 |
gwascentral | rs1448817 |
openSNP | rs1448817 |
23andMe | rs1448817 |
SNPshot | rs1448817 |
SNPdbe | rs1448817 |
MSV3d | rs1448817 |
GWAS Ctlg | rs1448817 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 26497660] Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF)