rs10489678
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10489678(A;A) |
| Make rs10489678(A;G) |
| Make rs10489678(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 1 |
| Position | 157699878 |
| Gene | FCRL3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10489678 |
| dbSNP (classic) | rs10489678 |
| ClinGen | rs10489678 |
| ebi | rs10489678 |
| HLI | rs10489678 |
| Exac | rs10489678 |
| Gnomad | rs10489678 |
| Varsome | rs10489678 |
| LitVar | rs10489678 |
| Map | rs10489678 |
| PheGenI | rs10489678 |
| Biobank | rs10489678 |
| 1000 genomes | rs10489678 |
| hgdp | rs10489678 |
| ensembl | rs10489678 |
| geneview | rs10489678 |
| scholar | rs10489678 |
| rs10489678 | |
| pharmgkb | rs10489678 |
| gwascentral | rs10489678 |
| openSNP | rs10489678 |
| 23andMe | rs10489678 |
| SNPshot | rs10489678 |
| SNPdbe | rs10489678 |
| MSV3d | rs10489678 |
| GWAS Ctlg | rs10489678 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 26051414] FCRL3 gene polymorphisms confer risk for sudden sensorineural hearing loss in a Chinese Han Population
