rs41314453
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs41314453(C;T) |
| Make rs41314453(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 9 |
| Position | 133442704 |
| Gene | ADAMTS13 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs41314453 |
| dbSNP (classic) | rs41314453 |
| ClinGen | rs41314453 |
| ebi | rs41314453 |
| HLI | rs41314453 |
| Exac | rs41314453 |
| Gnomad | rs41314453 |
| Varsome | rs41314453 |
| LitVar | rs41314453 |
| Map | rs41314453 |
| PheGenI | rs41314453 |
| Biobank | rs41314453 |
| 1000 genomes | rs41314453 |
| hgdp | rs41314453 |
| ensembl | rs41314453 |
| geneview | rs41314453 |
| scholar | rs41314453 |
| rs41314453 | |
| pharmgkb | rs41314453 |
| gwascentral | rs41314453 |
| openSNP | rs41314453 |
| 23andMe | rs41314453 |
| SNPshot | rs41314453 |
| SNPdbe | rs41314453 |
| MSV3d | rs41314453 |
| GWAS Ctlg | rs41314453 |
| Max Magnitude | 0 |
[PMID 25934476] Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity
| ClinVar | |
|---|---|
| Risk | rs41314453(T;T) |
| Alt | rs41314453(T;T) |
| Reference | Rs41314453(C;C) |
| Significance | Probable-non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | ADAMTS13 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000009.11:g.136307825C>T |
| CLNSRC | |
| CLNACC | RCV000220213.1, |
