rs8100085
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8100085(A;A) |
| Make rs8100085(A;T) |
| Make rs8100085(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 35032215 |
| Gene | SCN1B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8100085 |
| dbSNP (classic) | rs8100085 |
| ClinGen | rs8100085 |
| ebi | rs8100085 |
| HLI | rs8100085 |
| Exac | rs8100085 |
| Gnomad | rs8100085 |
| Varsome | rs8100085 |
| LitVar | rs8100085 |
| Map | rs8100085 |
| PheGenI | rs8100085 |
| Biobank | rs8100085 |
| 1000 genomes | rs8100085 |
| hgdp | rs8100085 |
| ensembl | rs8100085 |
| geneview | rs8100085 |
| scholar | rs8100085 |
| rs8100085 | |
| pharmgkb | rs8100085 |
| gwascentral | rs8100085 |
| openSNP | rs8100085 |
| 23andMe | rs8100085 |
| SNPshot | rs8100085 |
| SNPdbe | rs8100085 |
| MSV3d | rs8100085 |
| GWAS Ctlg | rs8100085 |
| GMAF | 0.3751 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21857919
] Evaluation of 15 functional candidate genes for association with chronic otitis media with effusion and/or recurrent otitis media (COME/ROM)
