rs759091617
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs759091617(A;A) |
| Make rs759091617(A;C) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 5 |
| Position | 146340275 |
| Gene | POU4F3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs759091617 |
| dbSNP (classic) | rs759091617 |
| ClinGen | rs759091617 |
| ebi | rs759091617 |
| HLI | rs759091617 |
| Exac | rs759091617 |
| Gnomad | rs759091617 |
| Varsome | rs759091617 |
| LitVar | rs759091617 |
| Map | rs759091617 |
| PheGenI | rs759091617 |
| Biobank | rs759091617 |
| 1000 genomes | rs759091617 |
| hgdp | rs759091617 |
| ensembl | rs759091617 |
| geneview | rs759091617 |
| scholar | rs759091617 |
| rs759091617 | |
| pharmgkb | rs759091617 |
| gwascentral | rs759091617 |
| openSNP | rs759091617 |
| 23andMe | rs759091617 |
| SNPshot | rs759091617 |
| SNPdbe | rs759091617 |
| MSV3d | rs759091617 |
| GWAS Ctlg | rs759091617 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs759091617(A;A) rs759091617(T;T) |
| Alt | rs759091617(A;A) rs759091617(T;T) |
| Reference | Rs759091617(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | POU4F3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000005.9:g.145719838C>T |
| CLNSRC | |
| CLNACC | RCV000171386.1, |
