rs16958477
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs16958477(A;A) |
| Make rs16958477(A;C) |
| Make rs16958477(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 73926125 |
| Gene | LOXL1, LOXL1-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16958477 |
| dbSNP (classic) | rs16958477 |
| ClinGen | rs16958477 |
| ebi | rs16958477 |
| HLI | rs16958477 |
| Exac | rs16958477 |
| Gnomad | rs16958477 |
| Varsome | rs16958477 |
| LitVar | rs16958477 |
| Map | rs16958477 |
| PheGenI | rs16958477 |
| Biobank | rs16958477 |
| 1000 genomes | rs16958477 |
| hgdp | rs16958477 |
| ensembl | rs16958477 |
| geneview | rs16958477 |
| scholar | rs16958477 |
| rs16958477 | |
| pharmgkb | rs16958477 |
| gwascentral | rs16958477 |
| openSNP | rs16958477 |
| 23andMe | rs16958477 |
| SNPshot | rs16958477 |
| SNPdbe | rs16958477 |
| MSV3d | rs16958477 |
| GWAS Ctlg | rs16958477 |
| GMAF | 0.2608 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 21212179
] LOXL1 promoter haplotypes are associated with exfoliation syndrome in a US Caucasian population
[PMID 20431720] Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population.
[PMID 26319397] LOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients
