rs752971070
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs752971070(-;-) |
| Make rs752971070(-;T) |
| Make rs752971070(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 2 |
| Position | 43800830 |
| Gene | DYNC2LI1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs752971070 |
| dbSNP (classic) | rs752971070 |
| ClinGen | rs752971070 |
| ebi | rs752971070 |
| HLI | rs752971070 |
| Exac | rs752971070 |
| Gnomad | rs752971070 |
| Varsome | rs752971070 |
| LitVar | rs752971070 |
| Map | rs752971070 |
| PheGenI | rs752971070 |
| Biobank | rs752971070 |
| 1000 genomes | rs752971070 |
| hgdp | rs752971070 |
| ensembl | rs752971070 |
| geneview | rs752971070 |
| scholar | rs752971070 |
| rs752971070 | |
| pharmgkb | rs752971070 |
| gwascentral | rs752971070 |
| openSNP | rs752971070 |
| 23andMe | rs752971070 |
| SNPshot | rs752971070 |
| SNPdbe | rs752971070 |
| MSV3d | rs752971070 |
| GWAS Ctlg | rs752971070 |
| Max Magnitude | 0 |
aka NM_016008.3(DYNC2LI1):c.655-11delT
OMIM pathogenic variant
