rs2306799
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2306799(A;A) |
Make rs2306799(A;G) |
Make rs2306799(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 43769889 |
Gene | KCNN4 |
is a | snp |
is | mentioned by |
dbSNP | rs2306799 |
dbSNP (classic) | rs2306799 |
ClinGen | rs2306799 |
ebi | rs2306799 |
HLI | rs2306799 |
Exac | rs2306799 |
Gnomad | rs2306799 |
Varsome | rs2306799 |
LitVar | rs2306799 |
Map | rs2306799 |
PheGenI | rs2306799 |
Biobank | rs2306799 |
1000 genomes | rs2306799 |
hgdp | rs2306799 |
ensembl | rs2306799 |
geneview | rs2306799 |
scholar | rs2306799 |
rs2306799 | |
pharmgkb | rs2306799 |
gwascentral | rs2306799 |
openSNP | rs2306799 |
23andMe | rs2306799 |
SNPshot | rs2306799 |
SNPdbe | rs2306799 |
MSV3d | rs2306799 |
GWAS Ctlg | rs2306799 |
GMAF | 0.2149 |
Max Magnitude | 0 |
[PMID 19644414] Relationship between haplotypes of KCNN4 gene and susceptibility to human vascular diseases in Japanese