rs574088829
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs574088829(A;A) |
| Make rs574088829(A;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 2 |
| Position | 39012319 |
| Gene | SOS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs574088829 |
| dbSNP (classic) | rs574088829 |
| ClinGen | rs574088829 |
| ebi | rs574088829 |
| HLI | rs574088829 |
| Exac | rs574088829 |
| Gnomad | rs574088829 |
| Varsome | rs574088829 |
| LitVar | rs574088829 |
| Map | rs574088829 |
| PheGenI | rs574088829 |
| Biobank | rs574088829 |
| 1000 genomes | rs574088829 |
| hgdp | rs574088829 |
| ensembl | rs574088829 |
| geneview | rs574088829 |
| scholar | rs574088829 |
| rs574088829 | |
| pharmgkb | rs574088829 |
| gwascentral | rs574088829 |
| openSNP | rs574088829 |
| 23andMe | rs574088829 |
| SNPshot | rs574088829 |
| SNPdbe | rs574088829 |
| MSV3d | rs574088829 |
| GWAS Ctlg | rs574088829 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs574088829(A;A) rs574088829(G;G) |
| Alt | rs574088829(A;A) rs574088829(G;G) |
| Reference | Rs574088829(T;T) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | SOS1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.39239460T>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000159127.1, |
