rs39335
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs39335(A;A) |
| Make rs39335(A;G) |
| Make rs39335(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 103813122 |
| Gene | RELN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs39335 |
| dbSNP (classic) | rs39335 |
| ClinGen | rs39335 |
| ebi | rs39335 |
| HLI | rs39335 |
| Exac | rs39335 |
| Gnomad | rs39335 |
| Varsome | rs39335 |
| LitVar | rs39335 |
| Map | rs39335 |
| PheGenI | rs39335 |
| Biobank | rs39335 |
| 1000 genomes | rs39335 |
| hgdp | rs39335 |
| ensembl | rs39335 |
| geneview | rs39335 |
| scholar | rs39335 |
| rs39335 | |
| pharmgkb | rs39335 |
| gwascentral | rs39335 |
| openSNP | rs39335 |
| 23andMe | rs39335 |
| SNPshot | rs39335 |
| SNPdbe | rs39335 |
| MSV3d | rs39335 |
| GWAS Ctlg | rs39335 |
| GMAF | 0.1676 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24227897
] The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population
[PMID 19230858] A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.
