Source: GWASCAT ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9644474
rs9644474
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0600139
Disease:
Prostate carcinoma
0.700 GeneticVariation GWASCAT Radiogenomics Consortium Genome-Wide Association Study Meta-Analysis of Late Toxicity After Prostate Cancer Radiotherapy. 31095341 2020
dbSNP: rs11166628
rs11166628
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs11166628
rs11166628
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0021704
Disease:
Intelligence
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs143593851
rs143593851
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0883409
Disease:
Cardiac troponin I measurement
A 0.700 GeneticVariation GWASCAT Cardiac Troponin T and Troponin I in the General Population. 31014085 2019
dbSNP: rs11166628
rs11166628
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0021704
Disease:
Intelligence
0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs11785202
rs11785202
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11785202
rs11785202
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4130250
rs4130250
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4323508
rs4323508
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4537336
rs4537336
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs4552942
rs4552942
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7819173
rs7819173
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7820672
rs7820672
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10505648
rs10505648
Entrez Id: 107986980
Gene Symbol: LINC02055
LINC02055
CUI: C0032460
Disease:
Polycystic Ovary Syndrome
A 0.700 GeneticVariation GWASCAT Genome-wide association study identified new susceptibility loci for polycystic ovary syndrome. 25574032 2015