rs772339721
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs772339721(A;T) |
| Make rs772339721(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 9 |
| Position | 99137964 |
| Gene | TGFBR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs772339721 |
| dbSNP (classic) | rs772339721 |
| ClinGen | rs772339721 |
| ebi | rs772339721 |
| HLI | rs772339721 |
| Exac | rs772339721 |
| Gnomad | rs772339721 |
| Varsome | rs772339721 |
| LitVar | rs772339721 |
| Map | rs772339721 |
| PheGenI | rs772339721 |
| Biobank | rs772339721 |
| 1000 genomes | rs772339721 |
| hgdp | rs772339721 |
| ensembl | rs772339721 |
| geneview | rs772339721 |
| scholar | rs772339721 |
| rs772339721 | |
| pharmgkb | rs772339721 |
| gwascentral | rs772339721 |
| openSNP | rs772339721 |
| 23andMe | rs772339721 |
| SNPshot | rs772339721 |
| SNPdbe | rs772339721 |
| MSV3d | rs772339721 |
| GWAS Ctlg | rs772339721 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs772339721(G;G) rs772339721(T;T) |
| Alt | rs772339721(G;G) rs772339721(T;T) |
| Reference | Rs772339721(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | TGFBR1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000009.11:g.101900246A>T |
| CLNSRC | |
| CLNACC | RCV000483348.1, |
