rs7081208
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Alzheimer's Disease
A
0.800
GeneticVariation
GWASCAT
Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease.
22430674
2013
rs7081208
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Alzheimer's Disease
0.800
GeneticVariation
GWASDB
Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease.
22430674
2013
rs11258533
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Red Blood Cell Count measurement
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs11258541
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Red cell distribution width determination
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs11258541
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
RDW - Red blood cell distribution width result
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs1887004
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Basal Cell Cancer
C
0.700
GeneticVariation
GWASCAT
Combined analysis of keratinocyte cancers identifies novel genome-wide loci.
31174203
2019
rs1887004
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Basal Cell Neoplasm
C
0.700
GeneticVariation
GWASCAT
Combined analysis of keratinocyte cancers identifies novel genome-wide loci.
31174203
2019
rs1887004
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Basal cell carcinoma
C
0.700
GeneticVariation
GWASCAT
Combined analysis of keratinocyte cancers identifies novel genome-wide loci.
31174203
2019
rs2169323
FRMD4A;LOC101928453
Body Height
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs17153734
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700
GeneticVariation
GWASCAT
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
30019117
2018
rs17153734
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Adolescent idiopathic scoliosis
0.700
GeneticVariation
GWASCAT
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
30019117
2018
rs10906522
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Breast Carcinoma
C
0.700
GeneticVariation
GWASCAT
Association analysis identifies 65 new breast cancer risk loci.
29059683
2017
rs10906564
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
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
rs11258564
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Red cell distribution width determination
G
0.700
GeneticVariation
GWASCAT
Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.
28957414
2017
rs11258564
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
RDW - Red blood cell distribution width result
G
0.700
GeneticVariation
GWASCAT
Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers.
28957414
2017
rs11258793
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
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
rs11258795
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
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
rs11258796
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
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
rs12570849
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Antiphospholipid Syndrome
C
0.700
GeneticVariation
GWASCAT
The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome.
28424481
2017
rs2292367
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
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
rs2446588
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
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
rs2446597
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
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
rs2457840
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
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
rs7074945
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
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
rs7074945
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
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