Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs760327
rs760327
Entrez Id: 6482
Gene Symbol: ST3GAL1
ST3GAL1
CUI: C1274700
Disease:
Postmenopausal frontal fibrosing alopecia
G 0.700 GeneticVariation GWASCAT Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02. 30850646 2019
dbSNP: rs760327
rs760327
Entrez Id: 6482
Gene Symbol: ST3GAL1
ST3GAL1
CUI: C4255374
Disease:
Frontal fibrosing alopecia
G 0.700 GeneticVariation GWASCAT Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02. 30850646 2019
dbSNP: rs7463447
rs7463447
Entrez Id: 6482
Gene Symbol: ST3GAL1
ST3GAL1
CUI: C2985280
Disease:
Blood Protein Measurement
G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs9643300
rs9643300
Entrez Id: 6482
Gene Symbol: ST3GAL1
ST3GAL1
CUI: C2985280
Disease:
Blood Protein Measurement
T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs9643297
rs9643297
Entrez Id: 6482
Gene Symbol: ST3GAL1
ST3GAL1
CUI: C0553723
Disease:
Squamous cell carcinoma of skin
0.010 GeneticVariation BEFREE Besides, we validated four other SNPs associated with SCC in the replication set, including rs9689649 in PARK2 gene (P = 2.7 × 10(-6) in combined set; P = 3.2 × 10(-5) in the discovery; and P = 0.02 in the replication), rs754626 in the SRC gene (P = 1.1 × 10(-6) in combined set; P = 1.4 × 10(-5) in the discovery and P = 0.02 in the replication), rs9643297 in ST3GAL1 gene (P = 8.2 × 10(-6) in combined set; P = 3.3 × 10(-5) in the discovery; and P = 0.04 in the replication), and rs17247181 in ERBB2IP gene (P = 4.2 × 10(-6) in combined set; P = 3.1 × 10(-5) in the discovery; and P = 0.048 in the replication). 26908436 2016
dbSNP: rs1048479
rs1048479
Entrez Id: 6482
Gene Symbol: ST3GAL1
ST3GAL1
CUI: C0021400
Disease:
Influenza
0.010 GeneticVariation BEFREE In a second phase of the study, the rs113350588 and rs1048479 polymorphisms identified in this sample were genotyped in a sample of 356 subjects from the northern and northeastern regions of Brazil with a diagnosis of pandemic influenza. 26436774 2015
dbSNP: rs113350588
rs113350588
Entrez Id: 6482
Gene Symbol: ST3GAL1
ST3GAL1
CUI: C0021400
Disease:
Influenza
0.010 GeneticVariation BEFREE In a second phase of the study, the rs113350588 and rs1048479 polymorphisms identified in this sample were genotyped in a sample of 356 subjects from the northern and northeastern regions of Brazil with a diagnosis of pandemic influenza. 26436774 2015