rs142410496
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common/normal |
| (A;G) | 5.5 | Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma |
| Make rs142410496(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 12 |
| Position | 55957137 |
| Gene | PMEL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs142410496 |
| dbSNP (classic) | rs142410496 |
| ClinGen | rs142410496 |
| ebi | rs142410496 |
| HLI | rs142410496 |
| Exac | rs142410496 |
| Gnomad | rs142410496 |
| Varsome | rs142410496 |
| LitVar | rs142410496 |
| Map | rs142410496 |
| PheGenI | rs142410496 |
| Biobank | rs142410496 |
| 1000 genomes | rs142410496 |
| hgdp | rs142410496 |
| ensembl | rs142410496 |
| geneview | rs142410496 |
| scholar | rs142410496 |
| rs142410496 | |
| pharmgkb | rs142410496 |
| gwascentral | rs142410496 |
| openSNP | rs142410496 |
| 23andMe | rs142410496 |
| SNPshot | rs142410496 |
| SNPdbe | rs142410496 |
| MSV3d | rs142410496 |
| GWAS Ctlg | rs142410496 |
| Max Magnitude | 5.5 |
aka c.1166T>C (p.Leu389Pro or L389P)
The variant allele is mentioned in a 2018 publication as a non-synonymous mutation in the PMEL gene, potentially acting in a dominant manner causing pigment dispersion syndrome (PDS) in the iris, which 15-20% of the time develops into pigmentary glaucoma (PG), a major cause of blindness in young adults.[PMID 30561643
]
