rs1805217
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1805217(C;C) |
Make rs1805217(C;T) |
Make rs1805217(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 9885601 |
is a | snp |
is | mentioned by |
dbSNP | rs1805217 |
dbSNP (classic) | rs1805217 |
ClinGen | rs1805217 |
ebi | rs1805217 |
HLI | rs1805217 |
Exac | rs1805217 |
Gnomad | rs1805217 |
Varsome | rs1805217 |
LitVar | rs1805217 |
Map | rs1805217 |
PheGenI | rs1805217 |
Biobank | rs1805217 |
1000 genomes | rs1805217 |
hgdp | rs1805217 |
ensembl | rs1805217 |
geneview | rs1805217 |
scholar | rs1805217 |
rs1805217 | |
pharmgkb | rs1805217 |
gwascentral | rs1805217 |
openSNP | rs1805217 |
23andMe | rs1805217 |
SNPshot | rs1805217 |
SNPdbe | rs1805217 |
MSV3d | rs1805217 |
GWAS Ctlg | rs1805217 |
Max Magnitude | 0 |
[PMID 23874724] KCNE1 rs1805127 Polymorphism Increases the Risk of Atrial Fibrillation: A Meta-Analysis of 10 Studies