Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6685931
rs6685931
CFHR4
0.710 GeneticVariation BEFREE The SNP rs6685931 in CFHR4 and its linked haplotype H1-2 also conferred a risk for AMD development, and therefore could be used to identify AMD patients who would benefit most from complement-inhibiting therapies. 29398083

2018
dbSNP: rs6685931
rs6685931
CFHR4
0.710 GeneticVariation GWASDB Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis. 23326517

2013
dbSNP: rs6685931
rs6685931
CFHR4
0.710 GeneticVariation GWASDB Sifting the wheat from the chaff: prioritizing GWAS results by identifying consistency across analytical methods. 22125219

2011