rs370296725
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs370296725(C;T) |
| Make rs370296725(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 16 |
| Position | 88717172 |
| Gene | MIR4722, PIEZO1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs370296725 |
| dbSNP (classic) | rs370296725 |
| ClinGen | rs370296725 |
| ebi | rs370296725 |
| HLI | rs370296725 |
| Exac | rs370296725 |
| Gnomad | rs370296725 |
| Varsome | rs370296725 |
| LitVar | rs370296725 |
| Map | rs370296725 |
| PheGenI | rs370296725 |
| Biobank | rs370296725 |
| 1000 genomes | rs370296725 |
| hgdp | rs370296725 |
| ensembl | rs370296725 |
| geneview | rs370296725 |
| scholar | rs370296725 |
| rs370296725 | |
| pharmgkb | rs370296725 |
| gwascentral | rs370296725 |
| openSNP | rs370296725 |
| 23andMe | rs370296725 |
| SNPshot | rs370296725 |
| SNPdbe | rs370296725 |
| MSV3d | rs370296725 |
| GWAS Ctlg | rs370296725 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs370296725(A;A) rs370296725(T;T) |
| Alt | rs370296725(A;A) rs370296725(T;T) |
| Reference | Rs370296725(C;C) |
| Significance | Pathogenic |
| Disease | Lymphedema |
| Variation | info |
| Gene | MIR4722 PIEZO1 |
| CLNDBN | Lymphedema, hereditary, III |
| Reversed | 0 |
| HGVS | NC_000016.9:g.88783580C>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000208749.2, |
