rs2231801
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 |
Make rs2231801(A;A) |
Make rs2231801(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 23360281 |
Gene | EFS |
is a | snp |
is | mentioned by |
dbSNP | rs2231801 |
dbSNP (classic) | rs2231801 |
ClinGen | rs2231801 |
ebi | rs2231801 |
HLI | rs2231801 |
Exac | rs2231801 |
Gnomad | rs2231801 |
Varsome | rs2231801 |
LitVar | rs2231801 |
Map | rs2231801 |
PheGenI | rs2231801 |
Biobank | rs2231801 |
1000 genomes | rs2231801 |
hgdp | rs2231801 |
ensembl | rs2231801 |
geneview | rs2231801 |
scholar | rs2231801 |
rs2231801 | |
pharmgkb | rs2231801 |
gwascentral | rs2231801 |
openSNP | rs2231801 |
23andMe | rs2231801 |
SNPshot | rs2231801 |
SNPdbe | rs2231801 |
MSV3d | rs2231801 |
GWAS Ctlg | rs2231801 |
GMAF | 0.005051 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21378987] A rare variant in MYH6 is associated with high risk of sick sinus syndrome.