rs1621
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs1621(A;A) |
| Make rs1621(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 116797552 |
| Gene | MET |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1621 |
| dbSNP (classic) | rs1621 |
| ClinGen | rs1621 |
| ebi | rs1621 |
| HLI | rs1621 |
| Exac | rs1621 |
| Gnomad | rs1621 |
| Varsome | rs1621 |
| LitVar | rs1621 |
| Map | rs1621 |
| PheGenI | rs1621 |
| Biobank | rs1621 |
| 1000 genomes | rs1621 |
| hgdp | rs1621 |
| ensembl | rs1621 |
| geneview | rs1621 |
| scholar | rs1621 |
| rs1621 | |
| pharmgkb | rs1621 |
| gwascentral | rs1621 |
| openSNP | rs1621 |
| 23andMe | rs1621 |
| SNPshot | rs1621 |
| SNPdbe | rs1621 |
| MSV3d | rs1621 |
| GWAS Ctlg | rs1621 |
| GMAF | 0.3012 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20416453] c-MET pathway involvement in chronic rhinosinusitis: a genetic association analysis
[PMID 19002214
] MET and autism susceptibility: family and case-control studies.
[PMID 19458495] Comprehensive analysis of the impact of SNPs and CNVs on human microRNAs and their regulatory genes.
[PMID 20011629] The hepatocyte growth factor receptor (MET) gene is not associated with refractive error and ocular biometrics in a Caucasian population.
[PMID 26649038] Association Analysis of MET Gene Polymorphism with Papillary Thyroid Carcinoma in a Chinese Population.
| ClinVar | |
|---|---|
| Risk | rs1621(A;A) |
| Alt | rs1621(A;A) |
| Reference | Rs1621(G;G) |
| Significance | Non-pathogenic |
| Disease | Renal cell carcinoma |
| Variation | info |
| Gene | MET |
| CLNDBN | Renal cell carcinoma, papillary, 1 |
| Reversed | 0 |
| HGVS | NC_000007.13:g.116437606G>A |
| CLNSRC | |
| CLNACC | RCV000300643.1, |
