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rs9938149

From SNPedia

Orientationplus
Stabilizedplus
Make rs9938149(A;A)
Make rs9938149(A;C)
Make rs9938149(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position88298034
is asnp
is mentioned by
dbSNPrs9938149
ebirs9938149
HLIrs9938149
Exacrs9938149
Varsomers9938149
Maprs9938149
PheGenIrs9938149
hapmaprs9938149
1000 genomesrs9938149
hgdprs9938149
ensemblrs9938149
gopubmedrs9938149
geneviewrs9938149
scholarrs9938149
googlers9938149
pharmgkbrs9938149
gwascentralrs9938149
openSNPrs9938149
23andMers9938149
23andMe allrs9938149
SNP Nexus

SNPshotrs9938149
SNPdbers9938149
MSV3drs9938149
GWAS Ctlgrs9938149
GMAF0.2567
Max Magnitude
? (A;A) (A;C) (C;C) 28

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


[PMID 22814818] Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness

[PMID 20485516OA-icon.png] Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.

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 2E-49
Odds Ratio .17 [0.15-0.19] unit increase


[PMID 24265017] Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian Population


[PMID 25675348] Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population