Source: GWASCAT

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 1 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 4 2012 2016
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: 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 1 2011 2013
dbSNP: rs9349379
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.760 1.000 5 2015 2019
dbSNP: rs9349379
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.710 1.000 1 2011 2015
dbSNP: rs9349379
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 3 2016 2019
dbSNP: rs11757278
rs11757278
PHACTR1
6 13180222 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11757634
rs11757634
PHACTR1
1.000 0.040 6 12964614 intron variant G/C snv 0.48
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1223397
rs1223397
TBC1D7 ; PHACTR1 ; TBC1D7-LOC100130357
6 13270713 intron variant G/A;C snv 0.19
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs17802893
rs17802893
PHACTR1 ; LOC107984015
6 12716327 upstream gene variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs4236091
rs4236091
PHACTR1
1.000 0.040 6 12951808 intron variant G/A snv 0.52
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4236093
rs4236093
PHACTR1
1.000 0.040 6 12957593 non coding transcript exon variant C/A;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4615376
rs4615376
PHACTR1
1.000 0.040 6 13070841 intron variant A/G snv 0.28
CUI: C3158111
Disease: response to SSRI
response to SSRI 		0.700 1.000 1 2015 2015
dbSNP: rs4615376
rs4615376
PHACTR1
1.000 0.040 6 13070841 intron variant A/G snv 0.28
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2015 2015
dbSNP: rs4714955
rs4714955
PHACTR1
1.000 0.040 6 12903203 intron variant C/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2014 2014
dbSNP: rs4714955
rs4714955
PHACTR1
1.000 0.040 6 12903203 intron variant C/A;T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2014 2014
dbSNP: rs4715016
rs4715016
PHACTR1
1.000 0.040 6 12963730 intron variant G/A snv 0.51
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4715023
rs4715023
PHACTR1
1.000 0.040 6 12967413 intron variant G/A snv 0.47
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6901563
rs6901563
PHACTR1
1.000 0.040 6 12983272 intron variant A/C snv 0.50
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6923878
rs6923878
PHACTR1
1.000 0.040 6 12969344 intron variant A/G snv 7.1E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017