FPR1, formyl peptide receptor 1, 2357

N. diseases: 93; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11666254
rs11666254
Entrez Id: 2357;2358
Gene Symbol: FPR1;FPR2
FPR1;FPR2
CUI: C0036690
Disease:
Septicemia 		0.010 GeneticVariation BEFREE The rs11666254 polymorphism in the FPR2/ALX gene is a functional SNP that increases sepsis susceptibility in patients after traumatic injury. 28679406 2017
dbSNP: rs11666254
rs11666254
Entrez Id: 2357;2358
Gene Symbol: FPR1;FPR2
FPR1;FPR2
CUI: C0243026
Disease:
Sepsis 		0.010 GeneticVariation BEFREE The rs11666254 polymorphism in the FPR2/ALX gene is a functional SNP that increases sepsis susceptibility in patients after traumatic injury. 28679406 2017
dbSNP: rs74256604
rs74256604
Entrez Id: 2357;2359
Gene Symbol: FPR1;FPR3
FPR1;FPR3
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018