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rs2721051

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs2721051(A;A)
Make rs2721051(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position40536747
GeneLOC100289058
is asnp
is mentioned by
dbSNPrs2721051
dbSNP (old)rs2721051
ClinGenrs2721051
ebirs2721051
HLIrs2721051
Exacrs2721051
Varsomers2721051
Maprs2721051
PheGenIrs2721051
Biobankrs2721051
1000 genomesrs2721051
hgdprs2721051
ensemblrs2721051
gopubmedrs2721051
geneviewrs2721051
scholarrs2721051
googlers2721051
pharmgkbrs2721051
gwascentralrs2721051
openSNPrs2721051
23andMers2721051
23andMe allrs2721051
SNP Nexus

SNPshotrs2721051
SNPdbers2721051
MSV3drs2721051
GWAS Ctlgrs2721051
GMAF0.07713
Max Magnitude0
? (A;A) (A;G) (G;G) 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 G
P-val 5E-10
Odds Ratio 0.24 [0.16-0.32] unit decrease
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 T
P-val 4E-14
Odds Ratio .17 [0.13-0.21] unit decrease


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