rs1536482
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1536482(A;A) |
Make rs1536482(A;G) |
Make rs1536482(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 134548682 |
is a | snp |
is | mentioned by |
dbSNP | rs1536482 |
dbSNP (classic) | rs1536482 |
ClinGen | rs1536482 |
ebi | rs1536482 |
HLI | rs1536482 |
Exac | rs1536482 |
Gnomad | rs1536482 |
Varsome | rs1536482 |
LitVar | rs1536482 |
Map | rs1536482 |
PheGenI | rs1536482 |
Biobank | rs1536482 |
1000 genomes | rs1536482 |
hgdp | rs1536482 |
ensembl | rs1536482 |
geneview | rs1536482 |
scholar | rs1536482 |
rs1536482 | |
pharmgkb | rs1536482 |
gwascentral | rs1536482 |
openSNP | rs1536482 |
23andMe | rs1536482 |
SNPshot | rs1536482 |
SNPdbe | rs1536482 |
MSV3d | rs1536482 |
GWAS Ctlg | rs1536482 |
GMAF | 0.3535 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20719862] New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8
GWAS snp | |
---|---|
PMID | [PMID 23291589] |
Trait | Corneal structure |
Title | Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. |
Risk Allele | A |
P-val | 3E-22 |
Odds Ratio | .12 [0.1-0.14] unit decrease |
GWAS snp | |
---|---|
PMID | [PMID 23493294] |
Trait | Central corneal thickness |
Title | A genome-wide association study of central corneal thickness in Latinos. |
Risk Allele | G |
P-val | 6E-8 |
Odds Ratio | .22 unit decrease |
[PMID 23513063] Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus.
[PMID 25675348] Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population