Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0030567
Disease:
Parkinson Disease
0.040 GeneticVariation BEFREE Our findings do not support the hypothesis of an interaction between the GRIN2A-rs4998386 or CYP1A2-rs762551 polymorphism and caffeine intake in determining PD risk. 29318639 2018
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0030567
Disease:
Parkinson Disease
0.040 GeneticVariation BEFREE We did not observe interactions for CYP1A2 rs762551 and rs2472304 in incident or prevalent PD. 28135712 2016
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0030567
Disease:
Parkinson Disease
0.040 GeneticVariation BEFREE CYP1A2 polymorphisms were not associated with PD risk; however, the coffee-PD association was strongest among subjects homozygous for either variant allele rs762551 (P(interaction) = 0.05) or rs2470890 (P(interaction) = 0.04). 21281405 2011
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0030567
Disease:
Parkinson Disease
0.040 GeneticVariation BEFREE The observed increased risk of PD among female but not male carriers of the rs762551 polymorphism of CYP1A2 and the interactions of caffeine with ESR1 rs3798577 and ESR2 rs1255998 may provide clues to explain the relationship between gender, caffeine intake, estrogen status and risk of PD and need to be replicated. 20304699 2010
dbSNP: rs2472304
rs2472304
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE We did not observe interactions for CYP1A2 rs762551 and rs2472304 in incident or prevalent PD. 28135712 2016
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE CYP1A2 polymorphisms were not associated with PD risk; however, the coffee-PD association was strongest among subjects homozygous for either variant allele rs762551 (P(interaction) = 0.05) or rs2470890 (P(interaction) = 0.04). 21281405 2011