rs752257333
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs752257333(A;A) |
| Make rs752257333(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 16 |
| Position | 89554486 |
| Gene | SPG7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs752257333 |
| dbSNP (classic) | rs752257333 |
| ClinGen | rs752257333 |
| ebi | rs752257333 |
| HLI | rs752257333 |
| Exac | rs752257333 |
| Gnomad | rs752257333 |
| Varsome | rs752257333 |
| LitVar | rs752257333 |
| Map | rs752257333 |
| PheGenI | rs752257333 |
| Biobank | rs752257333 |
| 1000 genomes | rs752257333 |
| hgdp | rs752257333 |
| ensembl | rs752257333 |
| geneview | rs752257333 |
| scholar | rs752257333 |
| rs752257333 | |
| pharmgkb | rs752257333 |
| gwascentral | rs752257333 |
| openSNP | rs752257333 |
| 23andMe | rs752257333 |
| SNPshot | rs752257333 |
| SNPdbe | rs752257333 |
| MSV3d | rs752257333 |
| GWAS Ctlg | rs752257333 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs752257333(A;A) |
| Alt | rs752257333(A;A) |
| Reference | Rs752257333(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | RPL13 SPG7 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000016.9:g.89620894G>A |
| CLNSRC | |
| CLNACC | RCV000200130.2, |
