Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2227341
rs2227341
Entrez Id: 9002
Gene Symbol: F2RL3
F2RL3
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs2227341
rs2227341
Entrez Id: 9002
Gene Symbol: F2RL3
F2RL3
CUI: C1445957
Disease:
Serum total cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs2227341
rs2227341
Entrez Id: 9002
Gene Symbol: F2RL3
F2RL3
CUI: C0428474
Disease:
Serum LDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs773902
rs773902
Entrez Id: 9002
Gene Symbol: F2RL3
F2RL3
CUI: C0038454
Disease:
Cerebrovascular accident 		0.010 GeneticVariation BEFREE A significant association of modest effect was detected between the rs773902 A allele and stroke. 30347494 2018
dbSNP: rs562764495
rs562764495
Entrez Id: 9002
Gene Symbol: F2RL3
F2RL3
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE SNP- and haplotype-based analysis showed that these two variants are associated with schizophrenia; there is an overrepresentation of RR homozygotes of P78R (OR=2.00, 95% CI=1.05-3.83) and MM homozygotes of I199M (OR=1.81, 95% CI=0.95-3.54) in schizophrenic patients as compared to control subjects. 18281137 2008