rs371717283
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 5 | Possible higher risk for intracranial aneurysm |
| (G;G) | 0 | common/normal |
| Make rs371717283(A;A) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 13 |
| Position | 52378012 |
| Gene | THSD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs371717283 |
| dbSNP (classic) | rs371717283 |
| ClinGen | rs371717283 |
| ebi | rs371717283 |
| HLI | rs371717283 |
| Exac | rs371717283 |
| Gnomad | rs371717283 |
| Varsome | rs371717283 |
| LitVar | rs371717283 |
| Map | rs371717283 |
| PheGenI | rs371717283 |
| Biobank | rs371717283 |
| 1000 genomes | rs371717283 |
| hgdp | rs371717283 |
| ensembl | rs371717283 |
| geneview | rs371717283 |
| scholar | rs371717283 |
| rs371717283 | |
| pharmgkb | rs371717283 |
| gwascentral | rs371717283 |
| openSNP | rs371717283 |
| 23andMe | rs371717283 |
| SNPshot | rs371717283 |
| SNPdbe | rs371717283 |
| MSV3d | rs371717283 |
| GWAS Ctlg | rs371717283 |
| Max Magnitude | 5 |
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
]
