rs2959656
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (G;G) | 0 | common genotype |
| Make rs2959656(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 64804546 |
| Gene | MAP4K2, MEN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2959656 |
| dbSNP (classic) | rs2959656 |
| ClinGen | rs2959656 |
| ebi | rs2959656 |
| HLI | rs2959656 |
| Exac | rs2959656 |
| Gnomad | rs2959656 |
| Varsome | rs2959656 |
| LitVar | rs2959656 |
| Map | rs2959656 |
| PheGenI | rs2959656 |
| Biobank | rs2959656 |
| 1000 genomes | rs2959656 |
| hgdp | rs2959656 |
| ensembl | rs2959656 |
| geneview | rs2959656 |
| scholar | rs2959656 |
| rs2959656 | |
| pharmgkb | rs2959656 |
| gwascentral | rs2959656 |
| openSNP | rs2959656 |
| 23andMe | rs2959656 |
| SNPshot | rs2959656 |
| SNPdbe | rs2959656 |
| MSV3d | rs2959656 |
| GWAS Ctlg | rs2959656 |
| GMAF | 0.1543 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| ClinVar | |
|---|---|
| Risk | Rs2959656(G;G) |
| Alt | Rs2959656(G;G) |
| Reference | Rs2959656(A;A) |
| Significance | Non-pathogenic |
| Disease | not provided not specified Multiple endocrine neoplasia Primary hyperparathyroidism |
| Variation | info |
| Gene | MAP4K2 MEN1 |
| CLNDBN | not provided not specified Multiple endocrine neoplasia, type 1 Primary hyperparathyroidism |
| Reversed | 1 |
| HGVS | NC_000011.9:g.64572018T\x3d; NC_000011.9:g.64572018T>C |
| CLNSRC | HGMD |
| CLNACC | RCV000034785.3, RCV000082334.6, RCV000204881.2, RCV000210359.1, RCV000121334.3, |
