rs16952059
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16952059(C;C) |
| Make rs16952059(C;T) |
| Make rs16952059(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 68425661 |
| Gene | ITGA11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16952059 |
| dbSNP (classic) | rs16952059 |
| ClinGen | rs16952059 |
| ebi | rs16952059 |
| HLI | rs16952059 |
| Exac | rs16952059 |
| Gnomad | rs16952059 |
| Varsome | rs16952059 |
| LitVar | rs16952059 |
| Map | rs16952059 |
| PheGenI | rs16952059 |
| Biobank | rs16952059 |
| 1000 genomes | rs16952059 |
| hgdp | rs16952059 |
| ensembl | rs16952059 |
| geneview | rs16952059 |
| scholar | rs16952059 |
| rs16952059 | |
| pharmgkb | rs16952059 |
| gwascentral | rs16952059 |
| openSNP | rs16952059 |
| 23andMe | rs16952059 |
| SNPshot | rs16952059 |
| SNPdbe | rs16952059 |
| MSV3d | rs16952059 |
| GWAS Ctlg | rs16952059 |
| GMAF | 0.1125 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22363784
] Challenges in Whole Exome Sequencing: An Example from Hereditary Deafness
