rs141724500
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs141724500(G;T) |
| Make rs141724500(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 20 |
| Position | 33438897 |
| Gene | SNTA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141724500 |
| dbSNP (classic) | rs141724500 |
| ClinGen | rs141724500 |
| ebi | rs141724500 |
| HLI | rs141724500 |
| Exac | rs141724500 |
| Gnomad | rs141724500 |
| Varsome | rs141724500 |
| LitVar | rs141724500 |
| Map | rs141724500 |
| PheGenI | rs141724500 |
| Biobank | rs141724500 |
| 1000 genomes | rs141724500 |
| hgdp | rs141724500 |
| ensembl | rs141724500 |
| geneview | rs141724500 |
| scholar | rs141724500 |
| rs141724500 | |
| pharmgkb | rs141724500 |
| gwascentral | rs141724500 |
| openSNP | rs141724500 |
| 23andMe | rs141724500 |
| SNPshot | rs141724500 |
| SNPdbe | rs141724500 |
| MSV3d | rs141724500 |
| GWAS Ctlg | rs141724500 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs141724500(A;A) rs141724500(T;T) |
| Alt | rs141724500(A;A) rs141724500(T;T) |
| Reference | Rs141724500(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided not specified |
| Variation | info |
| Gene | SNTA1 |
| CLNDBN | not provided not specified |
| Reversed | 0 |
| HGVS | NC_000020.10:g.32026703G>T |
| CLNSRC | |
| CLNACC | RCV000171113.3, RCV000185527.3, |
