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rs4711751

From SNPedia

Orientationplus
Stabilizedplus
Make rs4711751(C;C)
Make rs4711751(C;T)
Make rs4711751(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position43860845
is asnp
is mentioned by
dbSNPrs4711751
ebirs4711751
HLIrs4711751
Exacrs4711751
Varsomers4711751
Maprs4711751
PheGenIrs4711751
hapmaprs4711751
1000 genomesrs4711751
hgdprs4711751
ensemblrs4711751
gopubmedrs4711751
geneviewrs4711751
scholarrs4711751
googlers4711751
pharmgkbrs4711751
gwascentralrs4711751
openSNPrs4711751
23andMers4711751
23andMe allrs4711751
SNP Nexus

SNPshotrs4711751
SNPdbers4711751
MSV3drs4711751
GWAS Ctlgrs4711751
GMAF0.3489
Max Magnitude
GWAS snp
PMID [PMID 21665990OA-icon.png]
Trait
Title Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.
Risk Allele T
P-val 9E-9
Odds Ratio 1.1500 [NR]

[PMID 25228097] rs4711751 and rs1999930 Are Not Associated with Neovascular Age-Related Macular Degeneration or Polypoidal Choroidal Vasculopathy in the Chinese Population