Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9349379
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.820 1.000 4 2011 2019
dbSNP: rs12526453
rs12526453
PHACTR1
0.827 0.160 6 12927312 intron variant C/G snv 0.27
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.820 1.000 2 2011 2017
dbSNP: rs12526453
rs12526453
PHACTR1
0.827 0.160 6 12927312 intron variant C/G snv 0.27
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.820 1.000 1 2009 2015
dbSNP: rs9349379
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.810 1.000 1 2013 2016
dbSNP: rs9349379
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.800 1.000 2 2012 2016
dbSNP: rs9349379
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.800 1.000 2 2011 2013
dbSNP: rs1223397
rs1223397
TBC1D7 ; PHACTR1 ; TBC1D7-LOC100130357
6 13270713 intron variant G/A;C snv 0.19
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.800 1.000 1 2012 2012
dbSNP: rs1332844
rs1332844
PHACTR1
1.000 0.040 6 12888772 intron variant C/T snv 0.61
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2011 2011
dbSNP: rs12526453
rs12526453
PHACTR1
0.827 0.160 6 12927312 intron variant C/G snv 0.27
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.730 1.000 1 2013 2019
dbSNP: rs10807323
rs10807323
PHACTR1
6 12794799 intron variant G/A snv 0.34
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2011 2011
dbSNP: rs2026458
rs2026458
PHACTR1
0.882 0.080 6 12825642 intron variant C/T snv 0.34
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2011 2011
dbSNP: rs4711863
rs4711863
PHACTR1
6 12915185 intron variant G/C snv 0.29
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2011 2011
dbSNP: rs9369640
rs9369640
PHACTR1
0.851 0.080 6 12901209 intron variant C/A;G snv
CUI: C1842247
Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1 		0.700 1.000 1 2013 2013
dbSNP: rs9369640
rs9369640
PHACTR1
0.851 0.080 6 12901209 intron variant C/A;G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2014 2014