rs786204428
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (CAGG;CAGG) | 0 | common in clinvar |
| Make rs786204428(CAGG;TGTCCAAT) |
| Make rs786204428(TGTCCAAT;TGTCCAAT) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 3 |
| Position | 150972557 |
| Gene | CLRN1, CLRN1-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs786204428 |
| dbSNP (classic) | rs786204428 |
| ClinGen | rs786204428 |
| ebi | rs786204428 |
| HLI | rs786204428 |
| Exac | rs786204428 |
| Gnomad | rs786204428 |
| Varsome | rs786204428 |
| LitVar | rs786204428 |
| Map | rs786204428 |
| PheGenI | rs786204428 |
| Biobank | rs786204428 |
| 1000 genomes | rs786204428 |
| hgdp | rs786204428 |
| ensembl | rs786204428 |
| geneview | rs786204428 |
| scholar | rs786204428 |
| rs786204428 | |
| pharmgkb | rs786204428 |
| gwascentral | rs786204428 |
| openSNP | rs786204428 |
| 23andMe | rs786204428 |
| SNPshot | rs786204428 |
| SNPdbe | rs786204428 |
| MSV3d | rs786204428 |
| GWAS Ctlg | rs786204428 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs786204428(TGTCCAAT;TGTCCAAT) |
| Alt | rs786204428(TGTCCAAT;TGTCCAAT) |
| Reference | Rs786204428(CAGG;CAGG) |
| Significance | Other |
| Disease | Usher syndrome not provided |
| Variation | info |
| Gene | CLRN1-AS1 CLRN1 |
| CLNDBN | Usher syndrome, type 3A not provided |
| Reversed | 1 |
| HGVS | NC_000003.11:g.150690344_150690347delCCTGinsATTGGACA |
| CLNSRC | |
| CLNACC | RCV000169027.2, RCV000478734.1, |
