rs10967705
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10967705(C;C) |
Make rs10967705(C;G) |
Make rs10967705(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 2717922 |
Gene | KCNV2 |
is a | snp |
is | mentioned by |
dbSNP | rs10967705 |
dbSNP (classic) | rs10967705 |
ClinGen | rs10967705 |
ebi | rs10967705 |
HLI | rs10967705 |
Exac | rs10967705 |
Gnomad | rs10967705 |
Varsome | rs10967705 |
LitVar | rs10967705 |
Map | rs10967705 |
PheGenI | rs10967705 |
Biobank | rs10967705 |
1000 genomes | rs10967705 |
hgdp | rs10967705 |
ensembl | rs10967705 |
geneview | rs10967705 |
scholar | rs10967705 |
rs10967705 | |
pharmgkb | rs10967705 |
gwascentral | rs10967705 |
openSNP | rs10967705 |
23andMe | rs10967705 |
SNPshot | rs10967705 |
SNPdbe | rs10967705 |
MSV3d | rs10967705 |
GWAS Ctlg | rs10967705 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 30441785] The Impact of Potassium Channel Gene Polymorphisms on Antiepileptic Drug Responsiveness in Arab Patients with Epilepsy.