rs757725348
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs757725348(A;A) |
| Make rs757725348(A;C) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 14 |
| Position | 102033982 |
| Gene | DYNC1H1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs757725348 |
| dbSNP (classic) | rs757725348 |
| ClinGen | rs757725348 |
| ebi | rs757725348 |
| HLI | rs757725348 |
| Exac | rs757725348 |
| Gnomad | rs757725348 |
| Varsome | rs757725348 |
| LitVar | rs757725348 |
| Map | rs757725348 |
| PheGenI | rs757725348 |
| Biobank | rs757725348 |
| 1000 genomes | rs757725348 |
| hgdp | rs757725348 |
| ensembl | rs757725348 |
| geneview | rs757725348 |
| scholar | rs757725348 |
| rs757725348 | |
| pharmgkb | rs757725348 |
| gwascentral | rs757725348 |
| openSNP | rs757725348 |
| 23andMe | rs757725348 |
| SNPshot | rs757725348 |
| SNPdbe | rs757725348 |
| MSV3d | rs757725348 |
| GWAS Ctlg | rs757725348 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs757725348(A;A) rs757725348(T;T) |
| Alt | rs757725348(A;A) rs757725348(T;T) |
| Reference | Rs757725348(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DYNC1H1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000014.8:g.102500319C>T |
| CLNSRC | |
| CLNACC | RCV000235908.1, |
