rs10764319
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10764319(C;C) |
Make rs10764319(C;T) |
Make rs10764319(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 18139486 |
Gene | CACNB2 |
is a | snp |
is | mentioned by |
dbSNP | rs10764319 |
dbSNP (classic) | rs10764319 |
ClinGen | rs10764319 |
ebi | rs10764319 |
HLI | rs10764319 |
Exac | rs10764319 |
Gnomad | rs10764319 |
Varsome | rs10764319 |
LitVar | rs10764319 |
Map | rs10764319 |
PheGenI | rs10764319 |
Biobank | rs10764319 |
1000 genomes | rs10764319 |
hgdp | rs10764319 |
ensembl | rs10764319 |
geneview | rs10764319 |
scholar | rs10764319 |
rs10764319 | |
pharmgkb | rs10764319 |
gwascentral | rs10764319 |
openSNP | rs10764319 |
23andMe | rs10764319 |
SNPshot | rs10764319 |
SNPdbe | rs10764319 |
MSV3d | rs10764319 |
GWAS Ctlg | rs10764319 |
GMAF | 0.3705 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23744328] [Association between CACNB2 gene polymorphisms and essential hypertension]