rs145734330
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs145734330(A;A) |
| Make rs145734330(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 15930681 |
| Gene | SPEN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs145734330 |
| dbSNP (classic) | rs145734330 |
| ClinGen | rs145734330 |
| ebi | rs145734330 |
| HLI | rs145734330 |
| Exac | rs145734330 |
| Gnomad | rs145734330 |
| Varsome | rs145734330 |
| LitVar | rs145734330 |
| Map | rs145734330 |
| PheGenI | rs145734330 |
| Biobank | rs145734330 |
| 1000 genomes | rs145734330 |
| hgdp | rs145734330 |
| ensembl | rs145734330 |
| geneview | rs145734330 |
| scholar | rs145734330 |
| rs145734330 | |
| pharmgkb | rs145734330 |
| gwascentral | rs145734330 |
| openSNP | rs145734330 |
| 23andMe | rs145734330 |
| SNPshot | rs145734330 |
| SNPdbe | rs145734330 |
| MSV3d | rs145734330 |
| GWAS Ctlg | rs145734330 |
| Max Magnitude | 0 |
[PMID 21499247
] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
| ClinVar | |
|---|---|
| Risk | rs145734330(A;A) |
| Alt | rs145734330(A;A) |
| Reference | Rs145734330(G;G) |
| Significance | Untested |
| Disease | Malignant melanoma |
| Variation | info |
| Gene | SPEN |
| CLNDBN | Malignant melanoma |
| Reversed | 0 |
| HGVS | NC_000001.11:g.15930681G>A |
| CLNSRC | ClinVar |
| CLNACC | RCV000059971.2, |
