PHACTR1, phosphatase and actin regulator 1, 221692

N. diseases: 59; N. variants: 28
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0002949
Disease:
Aneurysm, Dissecting
0.010 GeneticVariation BEFREE The top variant, rs9349379, is intronic to PHACTR1, a risk locus for coronary artery disease, migraine, and cervical artery dissection. 27792790 2016
dbSNP: rs1223397
rs1223397
Entrez Id: 51256;221692;107080638
Gene Symbol: TBC1D7;PHACTR1;TBC1D7-LOC100130357
TBC1D7;PHACTR1;TBC1D7-LOC100130357
CUI: C0005823
Disease:
Blood Pressure
0.800 GeneticVariation GWASDB Genome-wide linkage and association scans for pulse pressure in Chinese twins. 22763476 2012
dbSNP: rs1223397
rs1223397
Entrez Id: 51256;221692;107080638
Gene Symbol: TBC1D7;PHACTR1;TBC1D7-LOC100130357
TBC1D7;PHACTR1;TBC1D7-LOC100130357
CUI: C0005823
Disease:
Blood Pressure
0.800 GeneticVariation GWASCAT Genome-wide linkage and association scans for pulse pressure in Chinese twins. 22763476 2012
dbSNP: rs11757278
rs11757278
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C1305855
Disease:
Body mass index
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs17802893
rs17802893
Entrez Id: 221692;107984015
Gene Symbol: PHACTR1;LOC107984015
PHACTR1;LOC107984015
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9367369
rs9367369
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C1305855
Disease:
Body mass index
A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs9395520
rs9395520
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C1611184
Disease:
Calcification of coronary artery
0.800 GeneticVariation GWASDB The second strongest association with CAC was with rs9349379 in the phosphatase and actin regulator 1 gene, PHACTR1, (Beta=0.30; 95% CI=0.22-0.40; p=4.67x10-11). 23394302 2013
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C1611184
Disease:
Calcification of coronary artery
A 0.800 GeneticVariation GWASCAT Genome-wide significant associations with CAC for SNPs on chromosome 9p21 near CDKN2A and CDKN2B (top SNP: rs1333049; P=7.58×10(-19)) and 6p24 (top SNP: rs9349379, within the PHACTR1 gene; P=2.65×10(-11)) replicated for CAC and for MI. 22144573 2011
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C1611184
Disease:
Calcification of coronary artery
A 0.800 GeneticVariation GWASDB Genome-wide significant associations with CAC for SNPs on chromosome 9p21 near CDKN2A and CDKN2B (top SNP: rs1333049; P=7.58×10(-19)) and 6p24 (top SNP: rs9349379, within the PHACTR1 gene; P=2.65×10(-11)) replicated for CAC and for MI. 22144573 2011
dbSNP: rs10807323
rs10807323
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C1611184
Disease:
Calcification of coronary artery
0.700 GeneticVariation GWASDB Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. 22144573 2011
dbSNP: rs2026458
rs2026458
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C1611184
Disease:
Calcification of coronary artery
0.700 GeneticVariation GWASDB Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. 22144573 2011
dbSNP: rs4711863
rs4711863
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C1611184
Disease:
Calcification of coronary artery
0.700 GeneticVariation GWASDB Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. 22144573 2011
dbSNP: rs2026458
rs2026458
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C4285890
Disease:
Carotid artery calcification
0.010 GeneticVariation BEFREE Among the four tested SNPs, rs2026458</span> was associated with calcification in both carotid artery (β = 0.31, 95% confidence interval [CI] 0.10-0.52, P = 0.003) and aortic arch (β = 0.32, 95% CI 0.10-0.54, P = 0.004), while rs1333049 was only associated with carotid artery calcification (β = 0.28, 95% CI 0.06-0.50, P = 0.011). 26071660 2015
dbSNP: rs2026458
rs2026458
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0577631
Disease:
Carotid Atherosclerosis
0.010 GeneticVariation BEFREE Our results suggest that PHACTR1 haplotypes inferred from the variants rs9349379, rs2026458 and rs2876300 affect PHACTR1 mRNA and bear the risk for CPP in patients with advanced carotid atherosclerosis. 31200082 2019
dbSNP: rs2876300
rs2876300
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0577631
Disease:
Carotid Atherosclerosis
0.010 GeneticVariation BEFREE Our results suggest that PHACTR1 haplotypes inferred from the variants rs9349379, rs2026458 and rs2876300 affect PHACTR1 mRNA and bear the risk for CPP in patients with advanced carotid atherosclerosis. 31200082 2019
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0577631
Disease:
Carotid Atherosclerosis
0.010 GeneticVariation BEFREE Our results suggest that PHACTR1 haplotypes inferred from the variants rs9349379, rs2026458 and rs2876300 affect PHACTR1 mRNA and bear the risk for CPP in patients with advanced carotid atherosclerosis. 31200082 2019
dbSNP: rs4714955
rs4714955
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0038454
Disease:
Cerebrovascular accident
0.700 GeneticVariation GWASCAT Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325 2014
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE The majority of published data in cervical artery dissection (CeAD), a common cause of stroke in young adults, derive from populations of European ancestry (EA), including a recent genome-wide study identifying an association with the rs9349379 polymorphism of the PHACTR1 gene. 30517918 2018
dbSNP: rs9357620
rs9357620
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0008810
Disease:
Circadian Rhythms
T 0.700 GeneticVariation GWASCAT GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person. 26835600 2016
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0338480
Disease:
Common Migraine
A 0.810 GeneticVariation GWASCAT Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. 27322543 2016
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0338480
Disease:
Common Migraine
0.810 GeneticVariation BEFREE Significant heterogeneity of SNP effects (p het < 1.4 × 10(-3)) was observed between the MA and MO subgroups (for SNP rs9349379), and between the clinic- and population-based subgroups (for SNPs rs10915437, rs6790925 and rs6478241). 25179292 2015
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0338480
Disease:
Common Migraine
0.810 GeneticVariation GWASDB Genome-wide meta-analysis identifies new susceptibility loci for migraine. 23793025 2013
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.020 GeneticVariation BEFREE The top variant, rs9349379, is intronic to PHACTR1, a risk locus for coronary artery disease, migraine, and cervical artery dissection. 27792790 2016
dbSNP: rs9349379
rs9349379
Entrez Id: 221692
Gene Symbol: PHACTR1
PHACTR1
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.020 GeneticVariation BEFREE Phosphatase and actin regulator 1 rs9349379 polymorphism is associated with an elevated susceptibility to coronary artery disease: a meta-analysis. 31278837 2019