rs2755237

Orientation

plus

Stabilized

plus

Make rs2755237(A;A)

Make rs2755237(A;C)

Make rs2755237(C;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

40535292

is a	snp
is	mentioned by
dbSNP	rs2755237
dbSNP (classic)	rs2755237
ClinGen	rs2755237
ebi	rs2755237
HLI	rs2755237
Exac	rs2755237
Gnomad	rs2755237
Varsome	rs2755237
LitVar	rs2755237
Map	rs2755237
PheGenI	rs2755237
Biobank	rs2755237
1000 genomes	rs2755237
hgdp	rs2755237
ensembl	rs2755237
geneview	rs2755237
scholar	rs2755237
google	rs2755237
pharmgkb	rs2755237
gwascentral	rs2755237
openSNP	rs2755237
23andMe	rs2755237
SNPshot	rs2755237
SNPdbe	rs2755237
MSV3d	rs2755237
GWAS Ctlg	rs2755237

GMAF

0.2328

Max Magnitude

0

?

(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 20485516 ] Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.