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rs11145951

From SNPedia

Orientationplus
Stabilizedplus
Make rs11145951(C;C)
Make rs11145951(C;T)
Make rs11145951(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position136965812
is asnp
is mentioned by
dbSNPrs11145951
ebirs11145951
HLIrs11145951
Exacrs11145951
Varsomers11145951
Maprs11145951
PheGenIrs11145951
hapmaprs11145951
1000 genomesrs11145951
hgdprs11145951
ensemblrs11145951
gopubmedrs11145951
geneviewrs11145951
scholarrs11145951
googlers11145951
pharmgkbrs11145951
gwascentralrs11145951
openSNPrs11145951
23andMers11145951
23andMe allrs11145951
SNP Nexus

SNPshotrs11145951
SNPdbers11145951
MSV3drs11145951
GWAS Ctlgrs11145951
GMAF0.3747
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 6E-12
Odds Ratio .09 [0.07-0.11] unit increase