rs760419
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs760419(A;A) |
Make rs760419(A;G) |
Make rs760419(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 2662127 |
Gene | KCNQ1, KCNQ1OT1 |
is a | snp |
is | mentioned by |
dbSNP | rs760419 |
dbSNP (classic) | rs760419 |
ClinGen | rs760419 |
ebi | rs760419 |
HLI | rs760419 |
Exac | rs760419 |
Gnomad | rs760419 |
Varsome | rs760419 |
LitVar | rs760419 |
Map | rs760419 |
PheGenI | rs760419 |
Biobank | rs760419 |
1000 genomes | rs760419 |
hgdp | rs760419 |
ensembl | rs760419 |
geneview | rs760419 |
scholar | rs760419 |
rs760419 | |
pharmgkb | rs760419 |
gwascentral | rs760419 |
openSNP | rs760419 |
23andMe | rs760419 |
SNPshot | rs760419 |
SNPdbe | rs760419 |
MSV3d | rs760419 |
GWAS Ctlg | rs760419 |
GMAF | 0.4959 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23651960] [KCNQ1 mutation in patients with lone atrial fibrillation]
[PMID 16839189] Human imprinted chromosomal regions are historical hot-spots of recombination.