rs7219669
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7219669(G;G) |
Make rs7219669(G;T) |
Make rs7219669(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 70525720 |
is a | snp |
is | mentioned by |
dbSNP | rs7219669 |
dbSNP (classic) | rs7219669 |
ClinGen | rs7219669 |
ebi | rs7219669 |
HLI | rs7219669 |
Exac | rs7219669 |
Gnomad | rs7219669 |
Varsome | rs7219669 |
LitVar | rs7219669 |
Map | rs7219669 |
PheGenI | rs7219669 |
Biobank | rs7219669 |
1000 genomes | rs7219669 |
hgdp | rs7219669 |
ensembl | rs7219669 |
geneview | rs7219669 |
scholar | rs7219669 |
rs7219669 | |
pharmgkb | rs7219669 |
gwascentral | rs7219669 |
openSNP | rs7219669 |
23andMe | rs7219669 |
SNPshot | rs7219669 |
SNPdbe | rs7219669 |
MSV3d | rs7219669 |
GWAS Ctlg | rs7219669 |
GMAF | 0.4568 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22342860![]() |
Trait | |
Title | A common variant near the KCNJ2 gene is associated with T-peak to T-end interval. |
Risk Allele | T |
P-val | 6E-14 |
Odds Ratio | 1.7000 None |