rs869025338
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA
CCCTGGGACTCCAG
0.700
CausalMutation
CLINVAR
rs41506144
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Cholelithiasis
0.700
GeneticVariation
GWASDB
A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.
17632509
2007
rs41506144
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Cholecystolithiasis
0.700
GeneticVariation
GWASDB
A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.
17632509
2007
rs1218412
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Serum albumin measurement
0.700
GeneticVariation
GWASDB
Genome-wide association study identifies multiple loci influencing human serum metabolite levels.
22286219
2012
rs4424567
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Nicotine Dependence
0.010
GeneticVariation
BEFREE
Also, we found two SNPs significantly associated with ND ; one in the FERM domain containing 4A (rs4424567 , p value(meta) = 2.30 × 10(-6)) and the other at 7q31.1 (rs848353, p value(meta) = 9.16 × 10(-8)).
22006218
2012
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
rs17314229
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Alzheimer's Disease
C
0.700
GeneticVariation
GWASCAT
Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease.
22430674
2013
rs2446581
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Alzheimer's Disease
A
0.700
GeneticVariation
GWASCAT
Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease.
22430674
2013
rs2457837
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Takayasu Arteritis
T
0.700
GeneticVariation
GWASCAT
Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study.
25604533
2015
rs12220909
FRMD4A;MIR4293
Squamous cell carcinoma of esophagus
0.020
GeneticVariation
BEFREE
This study provides the first evidence that miR-449b rs10061133 and miR-4293 rs12220909 are as sociated with ESCC risk in Chinese population.
26055141
2015
rs12220909
FRMD4A;MIR4293
Nasopharyngeal carcinoma
0.010
GeneticVariation
BEFREE
In this study, we analyzed associations between eight SNPs in miRNA mature sequences (i.e., rs3746444T>C in hsa-mir-499, rs4919510C>G in hsa-mir-608, rs13299349G>A in hsa-mir-3152, rs12220909G>C in hsa-mir-4293, rs2168518G>A in hsa-mir-4513, rs8078913T>C in hsa-mir-4520a, rs11237828T>C in hsa-mir-5579, and rs9295535T>C in hsa-mir-5689) and NPC susceptibility in southern China with 906 NPC cases and 1072 cancer-free controls, and validated the significant findings in eastern China with 684 cases and 907 healthy controls.
25861865
2015
rs12413816
FRMD4A;LOC105376426
RDW - Red blood cell distribution width result
T
0.700
GeneticVariation
GWASCAT
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
27863252
2016
rs12413816
FRMD4A;LOC105376426
Red cell distribution width determination
T
0.700
GeneticVariation
GWASCAT
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
27863252
2016
rs4750407
×
Entrez Id:
55691
Gene Symbol:
FRMD4A
FRMD4A
Goldenhar Syndrome
A
0.700
GeneticVariation
GWASCAT
Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
26853712
2016
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