rs6838973
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6838973(C;C) |
Make rs6838973(C;T) |
Make rs6838973(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 110844339 |
is a | snp |
is | mentioned by |
dbSNP | rs6838973 |
dbSNP (classic) | rs6838973 |
ClinGen | rs6838973 |
ebi | rs6838973 |
HLI | rs6838973 |
Exac | rs6838973 |
Gnomad | rs6838973 |
Varsome | rs6838973 |
LitVar | rs6838973 |
Map | rs6838973 |
PheGenI | rs6838973 |
Biobank | rs6838973 |
1000 genomes | rs6838973 |
hgdp | rs6838973 |
ensembl | rs6838973 |
geneview | rs6838973 |
scholar | rs6838973 |
rs6838973 | |
pharmgkb | rs6838973 |
gwascentral | rs6838973 |
openSNP | rs6838973 |
23andMe | rs6838973 |
SNPshot | rs6838973 |
SNPdbe | rs6838973 |
MSV3d | rs6838973 |
GWAS Ctlg | rs6838973 |
GMAF | 0.4086 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21760908] Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population