rs119486096
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs119486096(C;T) |
| Make rs119486096(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 10 |
| Position | 87505037 |
| Gene | MINPP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs119486096 |
| dbSNP (classic) | rs119486096 |
| ClinGen | rs119486096 |
| ebi | rs119486096 |
| HLI | rs119486096 |
| Exac | rs119486096 |
| Gnomad | rs119486096 |
| Varsome | rs119486096 |
| LitVar | rs119486096 |
| Map | rs119486096 |
| PheGenI | rs119486096 |
| Biobank | rs119486096 |
| 1000 genomes | rs119486096 |
| hgdp | rs119486096 |
| ensembl | rs119486096 |
| geneview | rs119486096 |
| scholar | rs119486096 |
| rs119486096 | |
| pharmgkb | rs119486096 |
| gwascentral | rs119486096 |
| openSNP | rs119486096 |
| 23andMe | rs119486096 |
| SNPshot | rs119486096 |
| SNPdbe | rs119486096 |
| MSV3d | rs119486096 |
| GWAS Ctlg | rs119486096 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs119486096(T;T) |
| Alt | rs119486096(T;T) |
| Reference | Rs119486096(C;C) |
| Significance | Pathogenic |
| Disease | Thyroid cancer |
| Variation | info |
| Gene | MINPP1 |
| CLNDBN | Thyroid cancer, follicular |
| Reversed | 0 |
| HGVS | NC_000010.10:g.89264794C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000005324.4, |
