rs11544238
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs11544238(G;G) |
| Make rs11544238(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 57476372 |
| Gene | ARHGAP9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11544238 |
| dbSNP (classic) | rs11544238 |
| ClinGen | rs11544238 |
| ebi | rs11544238 |
| HLI | rs11544238 |
| Exac | rs11544238 |
| Gnomad | rs11544238 |
| Varsome | rs11544238 |
| LitVar | rs11544238 |
| Map | rs11544238 |
| PheGenI | rs11544238 |
| Biobank | rs11544238 |
| 1000 genomes | rs11544238 |
| hgdp | rs11544238 |
| ensembl | rs11544238 |
| geneview | rs11544238 |
| scholar | rs11544238 |
| rs11544238 | |
| pharmgkb | rs11544238 |
| gwascentral | rs11544238 |
| openSNP | rs11544238 |
| 23andMe | rs11544238 |
| SNPshot | rs11544238 |
| SNPdbe | rs11544238 |
| MSV3d | rs11544238 |
| GWAS Ctlg | rs11544238 |
| GMAF | 0.4151 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19911011] Mutation of ARHGAP9 in patients with coronary spastic angina.
| ClinVar | |
|---|---|
| Risk | rs11544238(C;C) rs11544238(G;G) |
| Alt | rs11544238(C;C) rs11544238(G;G) |
| Reference | Rs11544238(T;T) |
| Significance | Other |
| Disease | Coronary artery spasm 3 |
| Variation | info |
| Gene | ARHGAP9 |
| CLNDBN | Coronary artery spasm 3, susceptibility to |
| Reversed | 1 |
| HGVS | NC_000012.11:g.57870155A>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000001248.5, |
