rs1005731602
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 3 |
| Position | 184373564 |
| Gene | THPO |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1005731602 |
| dbSNP (classic) | rs1005731602 |
| ClinGen | rs1005731602 |
| ebi | rs1005731602 |
| HLI | rs1005731602 |
| Exac | rs1005731602 |
| Gnomad | rs1005731602 |
| Varsome | rs1005731602 |
| LitVar | rs1005731602 |
| Map | rs1005731602 |
| PheGenI | rs1005731602 |
| Biobank | rs1005731602 |
| 1000 genomes | rs1005731602 |
| hgdp | rs1005731602 |
| ensembl | rs1005731602 |
| geneview | rs1005731602 |
| scholar | rs1005731602 |
| rs1005731602 | |
| pharmgkb | rs1005731602 |
| gwascentral | rs1005731602 |
| openSNP | rs1005731602 |
| 23andMe | rs1005731602 |
| SNPshot | rs1005731602 |
| SNPdbe | rs1005731602 |
| MSV3d | rs1005731602 |
| GWAS Ctlg | rs1005731602 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1005731602(T;T) |
| Alt | rs1005731602(T;T) |
| Reference | Rs1005731602(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000003.11:g.184091352C>T |
| CLNSRC | |
| CLNACC | RCV000414736.1, |
