rs745973997
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs745973997(A;A) |
| Make rs745973997(A;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 9 |
| Position | 2646435 |
| Gene | VLDLR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs745973997 |
| dbSNP (classic) | rs745973997 |
| ClinGen | rs745973997 |
| ebi | rs745973997 |
| HLI | rs745973997 |
| Exac | rs745973997 |
| Gnomad | rs745973997 |
| Varsome | rs745973997 |
| LitVar | rs745973997 |
| Map | rs745973997 |
| PheGenI | rs745973997 |
| Biobank | rs745973997 |
| 1000 genomes | rs745973997 |
| hgdp | rs745973997 |
| ensembl | rs745973997 |
| geneview | rs745973997 |
| scholar | rs745973997 |
| rs745973997 | |
| pharmgkb | rs745973997 |
| gwascentral | rs745973997 |
| openSNP | rs745973997 |
| 23andMe | rs745973997 |
| SNPshot | rs745973997 |
| SNPdbe | rs745973997 |
| MSV3d | rs745973997 |
| GWAS Ctlg | rs745973997 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs745973997(A;A) |
| Alt | rs745973997(A;A) |
| Reference | Rs745973997(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | VLDLR |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000009.11:g.2646435G>A |
| CLNSRC | |
| CLNACC | RCV000255297.1, |
