rs10500279
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs10500279(C;C) |
Make rs10500279(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 38544428 |
Gene | RYR1 |
is a | snp |
is | mentioned by |
dbSNP | rs10500279 |
dbSNP (classic) | rs10500279 |
ClinGen | rs10500279 |
ebi | rs10500279 |
HLI | rs10500279 |
Exac | rs10500279 |
Gnomad | rs10500279 |
Varsome | rs10500279 |
LitVar | rs10500279 |
Map | rs10500279 |
PheGenI | rs10500279 |
Biobank | rs10500279 |
1000 genomes | rs10500279 |
hgdp | rs10500279 |
ensembl | rs10500279 |
geneview | rs10500279 |
scholar | rs10500279 |
rs10500279 | |
pharmgkb | rs10500279 |
gwascentral | rs10500279 |
openSNP | rs10500279 |
23andMe | rs10500279 |
SNPshot | rs10500279 |
SNPdbe | rs10500279 |
MSV3d | rs10500279 |
GWAS Ctlg | rs10500279 |
GMAF | 0.07759 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 21828061] Common variants in RYR1 are associated with left ventricular hypertrophy assessed by electrocardiogram