rs137957386
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs137957386(A;A) |
| Make rs137957386(A;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 11027301 |
| Gene | MASP2, TARDBP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137957386 |
| dbSNP (classic) | rs137957386 |
| ClinGen | rs137957386 |
| ebi | rs137957386 |
| HLI | rs137957386 |
| Exac | rs137957386 |
| Gnomad | rs137957386 |
| Varsome | rs137957386 |
| LitVar | rs137957386 |
| Map | rs137957386 |
| PheGenI | rs137957386 |
| Biobank | rs137957386 |
| 1000 genomes | rs137957386 |
| hgdp | rs137957386 |
| ensembl | rs137957386 |
| geneview | rs137957386 |
| scholar | rs137957386 |
| rs137957386 | |
| pharmgkb | rs137957386 |
| gwascentral | rs137957386 |
| openSNP | rs137957386 |
| 23andMe | rs137957386 |
| SNPshot | rs137957386 |
| SNPdbe | rs137957386 |
| MSV3d | rs137957386 |
| GWAS Ctlg | rs137957386 |
| Max Magnitude | 0 |
[PMID 21499247
] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
| ClinVar | |
|---|---|
| Risk | rs137957386(A;A) rs137957386(C;C) |
| Alt | rs137957386(A;A) rs137957386(C;C) |
| Reference | Rs137957386(T;T) |
| Significance | Untested |
| Disease | Malignant melanoma |
| Variation | info |
| Gene | MASP2 |
| CLNDBN | Malignant melanoma |
| Reversed | 0 |
| HGVS | NC_000001.11:g.11027301T>A |
| CLNSRC | ClinVar |
| CLNACC | RCV000059831.2, |
