rs756181906
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs756181906(G;T) |
| Make rs756181906(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 16 |
| Position | 2496828 |
| Gene | TBC1D24 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs756181906 |
| dbSNP (classic) | rs756181906 |
| ClinGen | rs756181906 |
| ebi | rs756181906 |
| HLI | rs756181906 |
| Exac | rs756181906 |
| Gnomad | rs756181906 |
| Varsome | rs756181906 |
| LitVar | rs756181906 |
| Map | rs756181906 |
| PheGenI | rs756181906 |
| Biobank | rs756181906 |
| 1000 genomes | rs756181906 |
| hgdp | rs756181906 |
| ensembl | rs756181906 |
| geneview | rs756181906 |
| scholar | rs756181906 |
| rs756181906 | |
| pharmgkb | rs756181906 |
| gwascentral | rs756181906 |
| openSNP | rs756181906 |
| 23andMe | rs756181906 |
| SNPshot | rs756181906 |
| SNPdbe | rs756181906 |
| MSV3d | rs756181906 |
| GWAS Ctlg | rs756181906 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs756181906(A;A) rs756181906(T;T) |
| Alt | rs756181906(A;A) rs756181906(T;T) |
| Reference | Rs756181906(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | TBC1D24 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000016.9:g.2546829G>T |
| CLNSRC | |
| CLNACC | RCV000189690.2, |
