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rs1536482

From SNPedia

Orientationplus
Stabilizedplus
Make rs1536482(A;A)
Make rs1536482(A;G)
Make rs1536482(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position134548682
is asnp
is mentioned by
dbSNPrs1536482
ebirs1536482
HLIrs1536482
Exacrs1536482
Varsomers1536482
Maprs1536482
PheGenIrs1536482
hapmaprs1536482
1000 genomesrs1536482
hgdprs1536482
ensemblrs1536482
gopubmedrs1536482
geneviewrs1536482
scholarrs1536482
googlers1536482
pharmgkbrs1536482
gwascentralrs1536482
openSNPrs1536482
23andMers1536482
23andMe allrs1536482
SNP Nexus

SNPshotrs1536482
SNPdbers1536482
MSV3drs1536482
GWAS Ctlgrs1536482
GMAF0.3535
Max Magnitude
? (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 23291589OA-icon.png]
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 23493294OA-icon.png]
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 23513063OA-icon.png] 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