rs9349379, PHACTR1

N. diseases: 8
Source: GWASCAT ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
169 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.820 1.000 4 2011 2019
Common Migraine
CUI: C0338480
Disease: Common Migraine
9 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.810 1.000 1 2013 2016
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
114 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.800 1.000 4 2012 2016
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
84 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.800 1.000 1 2011 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
551 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.760 1.000 5 2015 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
58 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.710 1.000 1 2011 2015
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.700 1.000 3 2016 2019
Headache
CUI: C0018681
Disease: Headache
28 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.700 1.000 1 2018 2018