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rs2755237

From SNPedia

Orientationplus
Stabilizedplus
Make rs2755237(A;A)
Make rs2755237(A;C)
Make rs2755237(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position40535292
is asnp
is mentioned by
dbSNPrs2755237
ebirs2755237
HLIrs2755237
Exacrs2755237
Varsomers2755237
Maprs2755237
PheGenIrs2755237
hapmaprs2755237
1000 genomesrs2755237
hgdprs2755237
ensemblrs2755237
gopubmedrs2755237
geneviewrs2755237
scholarrs2755237
googlers2755237
pharmgkbrs2755237
gwascentralrs2755237
openSNPrs2755237
23andMers2755237
23andMe allrs2755237
SNP Nexus

SNPshotrs2755237
SNPdbers2755237
MSV3drs2755237
GWAS Ctlgrs2755237
GMAF0.2328
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20719862]
Trait
Title New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8
Risk Allele A
P-val 1E-8
Odds Ratio 0.17 [0.11-0.23] unit increase


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