FCRL3, Fc receptor like 3, 115352

N. diseases: 62; N. variants: 13
Disease: Graves Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3761959
rs3761959
Entrez Id: 115352
Gene Symbol: FCRL3
FCRL3
CUI: C0018213
Disease:
Graves Disease 		0.810 GeneticVariation BEFREE Moreover, the haplotypes with the risk allele A of rs3761959 and risk allele C of rs7528684 were associated with GD risk. 23505439 2013
dbSNP: rs3761959
rs3761959
Entrez Id: 115352
Gene Symbol: FCRL3
FCRL3
CUI: C0018213
Disease:
Graves Disease 		A 0.810 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011
dbSNP: rs3761959
rs3761959
Entrez Id: 115352
Gene Symbol: FCRL3
FCRL3
CUI: C0018213
Disease:
Graves Disease 		A 0.810 GeneticVariation GWASCAT A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011