rs780150341
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs780150341(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 13 |
| Position | 52377647 |
| Gene | THSD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs780150341 |
| dbSNP (classic) | rs780150341 |
| ClinGen | rs780150341 |
| ebi | rs780150341 |
| HLI | rs780150341 |
| Exac | rs780150341 |
| Gnomad | rs780150341 |
| Varsome | rs780150341 |
| LitVar | rs780150341 |
| Map | rs780150341 |
| PheGenI | rs780150341 |
| Biobank | rs780150341 |
| 1000 genomes | rs780150341 |
| hgdp | rs780150341 |
| ensembl | rs780150341 |
| geneview | rs780150341 |
| scholar | rs780150341 |
| rs780150341 | |
| pharmgkb | rs780150341 |
| gwascentral | rs780150341 |
| openSNP | rs780150341 |
| 23andMe | rs780150341 |
| SNPshot | rs780150341 |
| SNPdbe | rs780150341 |
| MSV3d | rs780150341 |
| GWAS Ctlg | rs780150341 |
| Max Magnitude | 0 |
This SNP represents a rare variant in the THSD1 gene on chromosome 13.
The minor allele has been reported (in heterozygotes) in a 2016 study to be potentially strongly associated with intracranial Aneurysm.[PMID 27895300
]
