rs1060499536
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (A;A) | 0 | common in clinvar | 
| Make rs1060499536(A;G) | 
| Make rs1060499536(G;G) | 
| Reference | GRCh38.p7 38.3/150 | 
| Chromosome | 5 | 
| Position | 149896778 | 
| Gene | PDE6A | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs1060499536 | 
| dbSNP (classic) | rs1060499536 | 
| ClinGen | rs1060499536 | 
| ebi | rs1060499536 | 
| HLI | rs1060499536 | 
| Exac | rs1060499536 | 
| Gnomad | rs1060499536 | 
| Varsome | rs1060499536 | 
| LitVar | rs1060499536 | 
| Map | rs1060499536 | 
| PheGenI | rs1060499536 | 
| Biobank | rs1060499536 | 
| 1000 genomes | rs1060499536 | 
| hgdp | rs1060499536 | 
| ensembl | rs1060499536 | 
| geneview | rs1060499536 | 
| scholar | rs1060499536 | 
| rs1060499536 | |
| pharmgkb | rs1060499536 | 
| gwascentral | rs1060499536 | 
| openSNP | rs1060499536 | 
| 23andMe | rs1060499536 | 
| SNPshot | rs1060499536 | 
| SNPdbe | rs1060499536 | 
| MSV3d | rs1060499536 | 
| GWAS Ctlg | rs1060499536 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs1060499536(G;G) | 
| Alt | rs1060499536(G;G) | 
| Reference | Rs1060499536(A;A) | 
| Significance | Pathogenic | 
| Disease | Retinitis pigmentosa 43 | 
| Variation | info | 
| Gene | PDE6A | 
| CLNDBN | Retinitis pigmentosa 43 | 
| Reversed | 1 | 
| HGVS | NC_000005.9:g.149276341T>C | 
| CLNSRC | OMIM Allelic Variant | 
| CLNACC | RCV000210743.1, | 
