rs199740930
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs199740930(C;T) |
| Make rs199740930(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 6 |
| Position | 65057613 |
| Gene | EYS |
| is a | snp |
| is | mentioned by |
| dbSNP | rs199740930 |
| dbSNP (classic) | rs199740930 |
| ClinGen | rs199740930 |
| ebi | rs199740930 |
| HLI | rs199740930 |
| Exac | rs199740930 |
| Gnomad | rs199740930 |
| Varsome | rs199740930 |
| LitVar | rs199740930 |
| Map | rs199740930 |
| PheGenI | rs199740930 |
| Biobank | rs199740930 |
| 1000 genomes | rs199740930 |
| hgdp | rs199740930 |
| ensembl | rs199740930 |
| geneview | rs199740930 |
| scholar | rs199740930 |
| rs199740930 | |
| pharmgkb | rs199740930 |
| gwascentral | rs199740930 |
| openSNP | rs199740930 |
| 23andMe | rs199740930 |
| 23andMe all | rs199740930 |
| SNPshot | rs199740930 |
| SNPdbe | rs199740930 |
| MSV3d | rs199740930 |
| GWAS Ctlg | rs199740930 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs199740930(T;T) |
| Alt | rs199740930(T;T) |
| Reference | Rs199740930(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | EYS |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000006.11:g.65767506C>T |
| CLNSRC | |
| CLNACC | RCV000484533.2, |
