rs782623477
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs782623477(A;A) |
| Make rs782623477(A;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 9 |
| Position | 133352509 |
| Gene | SURF1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs782623477 |
| dbSNP (classic) | rs782623477 |
| ClinGen | rs782623477 |
| ebi | rs782623477 |
| HLI | rs782623477 |
| Exac | rs782623477 |
| Gnomad | rs782623477 |
| Varsome | rs782623477 |
| LitVar | rs782623477 |
| Map | rs782623477 |
| PheGenI | rs782623477 |
| Biobank | rs782623477 |
| 1000 genomes | rs782623477 |
| hgdp | rs782623477 |
| ensembl | rs782623477 |
| geneview | rs782623477 |
| scholar | rs782623477 |
| rs782623477 | |
| pharmgkb | rs782623477 |
| gwascentral | rs782623477 |
| openSNP | rs782623477 |
| 23andMe | rs782623477 |
| SNPshot | rs782623477 |
| SNPdbe | rs782623477 |
| MSV3d | rs782623477 |
| GWAS Ctlg | rs782623477 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs782623477(A;A) |
| Alt | rs782623477(A;A) |
| Reference | Rs782623477(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | SURF1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000009.11:g.136219364G>A |
| CLNSRC | |
| CLNACC | RCV000321649.1, |
