rs138459502
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs138459502(C;C) |
| Make rs138459502(C;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 2 |
| Position | 39023159 |
| Gene | SOS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs138459502 |
| dbSNP (classic) | rs138459502 |
| ClinGen | rs138459502 |
| ebi | rs138459502 |
| HLI | rs138459502 |
| Exac | rs138459502 |
| Gnomad | rs138459502 |
| Varsome | rs138459502 |
| LitVar | rs138459502 |
| Map | rs138459502 |
| PheGenI | rs138459502 |
| Biobank | rs138459502 |
| 1000 genomes | rs138459502 |
| hgdp | rs138459502 |
| ensembl | rs138459502 |
| geneview | rs138459502 |
| scholar | rs138459502 |
| rs138459502 | |
| pharmgkb | rs138459502 |
| gwascentral | rs138459502 |
| openSNP | rs138459502 |
| 23andMe | rs138459502 |
| SNPshot | rs138459502 |
| SNPdbe | rs138459502 |
| MSV3d | rs138459502 |
| GWAS Ctlg | rs138459502 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs138459502(A;A) rs138459502(C;C) |
| Alt | rs138459502(A;A) rs138459502(C;C) |
| Reference | Rs138459502(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not specified not provided |
| Variation | info |
| Gene | SOS1 |
| CLNDBN | not specified not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.39250300G>A; NC_000002.11:g.39250300G>C |
| CLNSRC | |
| CLNACC | RCV000421562.1, RCV000159188.2, |
