rs11191692
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11191692(A;A) |
| Make rs11191692(A;G) |
| Make rs11191692(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 103454008 |
| Gene | CALHM1, CALHM2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11191692 |
| dbSNP (classic) | rs11191692 |
| ClinGen | rs11191692 |
| ebi | rs11191692 |
| HLI | rs11191692 |
| Exac | rs11191692 |
| Gnomad | rs11191692 |
| Varsome | rs11191692 |
| LitVar | rs11191692 |
| Map | rs11191692 |
| PheGenI | rs11191692 |
| Biobank | rs11191692 |
| 1000 genomes | rs11191692 |
| hgdp | rs11191692 |
| ensembl | rs11191692 |
| geneview | rs11191692 |
| scholar | rs11191692 |
| rs11191692 | |
| pharmgkb | rs11191692 |
| gwascentral | rs11191692 |
| openSNP | rs11191692 |
| 23andMe | rs11191692 |
| SNPshot | rs11191692 |
| SNPdbe | rs11191692 |
| MSV3d | rs11191692 |
| GWAS Ctlg | rs11191692 |
| GMAF | 0.2828 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24326043] No association between polymorphisms in the calcium homeostasis modulator 1 gene and mesial temporal lobe epilepsy risk in a Chinese population
[PMID 21439911] A polymorphism in CALHM1 is associated with temporal lobe epilepsy.
