rs754645487
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs754645487(A;A) |
| Make rs754645487(A;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 10 |
| Position | 122462103 |
| Gene | HTRA1, LOC105378525 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs754645487 |
| dbSNP (classic) | rs754645487 |
| ClinGen | rs754645487 |
| ebi | rs754645487 |
| HLI | rs754645487 |
| Exac | rs754645487 |
| Gnomad | rs754645487 |
| Varsome | rs754645487 |
| LitVar | rs754645487 |
| Map | rs754645487 |
| PheGenI | rs754645487 |
| Biobank | rs754645487 |
| 1000 genomes | rs754645487 |
| hgdp | rs754645487 |
| ensembl | rs754645487 |
| geneview | rs754645487 |
| scholar | rs754645487 |
| rs754645487 | |
| pharmgkb | rs754645487 |
| gwascentral | rs754645487 |
| openSNP | rs754645487 |
| 23andMe | rs754645487 |
| SNPshot | rs754645487 |
| SNPdbe | rs754645487 |
| MSV3d | rs754645487 |
| GWAS Ctlg | rs754645487 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs754645487(A;A) rs754645487(T;T) |
| Alt | rs754645487(A;A) rs754645487(T;T) |
| Reference | Rs754645487(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | HTRA1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.124221619C>T |
| CLNSRC | |
| CLNACC | RCV000487710.1, |
