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rs4961511

From SNPedia

Orientationplus
Stabilizedplus
Make rs4961511(G;G)
Make rs4961511(G;T)
Make rs4961511(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position16970811
is asnp
is mentioned by
dbSNPrs4961511
ebirs4961511
HLIrs4961511
Exacrs4961511
Varsomers4961511
Maprs4961511
PheGenIrs4961511
hapmaprs4961511
1000 genomesrs4961511
hgdprs4961511
ensemblrs4961511
gopubmedrs4961511
geneviewrs4961511
scholarrs4961511
googlers4961511
pharmgkbrs4961511
gwascentralrs4961511
openSNPrs4961511
23andMers4961511
23andMe allrs4961511
SNP Nexus

SNPshotrs4961511
SNPdbers4961511
MSV3drs4961511
GWAS Ctlgrs4961511
GMAF0.4215
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23322567OA-icon.png]
Trait Corneal astigmatism
Title Identification of a candidate gene for astigmatism.
Risk Allele G
P-val 9E-6
Odds Ratio .05 [NR] unit increase