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rs12447690

From SNPedia

Orientationplus
Stabilizedplus
Make rs12447690(C;C)
Make rs12447690(C;T)
Make rs12447690(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position88264518
is asnp
is mentioned by
dbSNPrs12447690
ebirs12447690
HLIrs12447690
Exacrs12447690
Varsomers12447690
Maprs12447690
PheGenIrs12447690
hapmaprs12447690
1000 genomesrs12447690
hgdprs12447690
ensemblrs12447690
gopubmedrs12447690
geneviewrs12447690
scholarrs12447690
googlers12447690
pharmgkbrs12447690
gwascentralrs12447690
openSNPrs12447690
23andMers12447690
23andMe allrs12447690
SNP Nexus

SNPshotrs12447690
SNPdbers12447690
MSV3drs12447690
GWAS Ctlgrs12447690
GMAF0.4128
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20485516OA-icon.png]
Trait Central corneal thickness
Title Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness
Risk Allele C
P-val 9E-11
Odds Ratio 0.16 [0.10-0.22] unit increase
GWAS snp
PMID [PMID 20719862]
Trait
Title New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8
Risk Allele G
P-val 6E-22
Odds Ratio 0.16 [0.13-0.19] unit decrease

[PMID 21098505] Collagen related genes influence glaucoma risk factor, central corneal thickness


[PMID 22661486OA-icon.png] Genome-wide Analysis of Central Corneal Thickness in Primary Open-angle Glaucoma Cases in the NEIGHBOR and GLAUGEN consortia