rs6426929
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6426929(A;A) |
Make rs6426929(A;G) |
Make rs6426929(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 154778513 |
Gene | KCNN3 |
is a | snp |
is | mentioned by |
dbSNP | rs6426929 |
dbSNP (classic) | rs6426929 |
ClinGen | rs6426929 |
ebi | rs6426929 |
HLI | rs6426929 |
Exac | rs6426929 |
Gnomad | rs6426929 |
Varsome | rs6426929 |
LitVar | rs6426929 |
Map | rs6426929 |
PheGenI | rs6426929 |
Biobank | rs6426929 |
1000 genomes | rs6426929 |
hgdp | rs6426929 |
ensembl | rs6426929 |
geneview | rs6426929 |
scholar | rs6426929 |
rs6426929 | |
pharmgkb | rs6426929 |
gwascentral | rs6426929 |
openSNP | rs6426929 |
23andMe | rs6426929 |
SNPshot | rs6426929 |
SNPdbe | rs6426929 |
MSV3d | rs6426929 |
GWAS Ctlg | rs6426929 |
GMAF | 0.4229 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22030984] Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate