Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1043618
rs1043618
Entrez Id: 3303;3305
Gene Symbol: HSPA1A;HSPA1L
HSPA1A;HSPA1L
CUI: C1800706
Disease:
Idiopathic Pulmonary Fibrosis
0.010 GeneticVariation BEFREE Our findings indicate that HSPA1B (rs1061581), HSPA1L (rs2227956) and HSPA1 (rs1043618) polymorphisms are associated with a decreased risk of IPF. 26496868 2015
dbSNP: rs1061581
rs1061581
Entrez Id: 3303;3305
Gene Symbol: HSPA1A;HSPA1L
HSPA1A;HSPA1L
CUI: C1800706
Disease:
Idiopathic Pulmonary Fibrosis
0.010 GeneticVariation BEFREE Our findings indicate that HSPA1B (rs1061581), HSPA1L (rs2227956) and HSPA1 (rs1043618) polymorphisms are associated with a decreased risk of IPF. 26496868 2015
dbSNP: rs2075800
rs2075800
Entrez Id: 3305
Gene Symbol: HSPA1L
HSPA1L
CUI: C1800706
Disease:
Idiopathic Pulmonary Fibrosis
0.010 GeneticVariation BEFREE In contrast, the HSPA1L (rs2075800) TT genotype was associated with susceptibility to IPF (OR = 2.52, 95 % CI = 1.32-4.81; p = 0.005). 26496868 2015
dbSNP: rs2227956
rs2227956
Entrez Id: 3305
Gene Symbol: HSPA1L
HSPA1L
CUI: C1800706
Disease:
Idiopathic Pulmonary Fibrosis
0.010 GeneticVariation BEFREE Our findings indicate that HSPA1B (rs1061581), HSPA1L (rs2227956) and HSPA1 (rs1043618) polymorphisms are associated with a decreased risk of IPF. 26496868 2015