rs10128898
×
Entrez Id:
23085
Gene Symbol:
ERC1
ERC1
Body Height
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs12298813
×
Entrez Id:
23085
Gene Symbol:
ERC1
ERC1
Vital capacity
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs7971674
×
Entrez Id:
23085
Gene Symbol:
ERC1
ERC1
Body Height
T
0.700
GeneticVariation
GWASCAT
Evaluation and application of summary statistic imputation to discover new height-associated loci.
29782485
2018
rs12301937
×
Entrez Id:
23085
Gene Symbol:
ERC1
ERC1
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
rs12321803
×
Entrez Id:
23085
Gene Symbol:
ERC1
ERC1
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
rs6489283
×
Entrez Id:
23085
Gene Symbol:
ERC1
ERC1
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
rs766095
×
Entrez Id:
23085
Gene Symbol:
ERC1
ERC1
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
rs7968583
×
Entrez Id:
23085
Gene Symbol:
ERC1
ERC1
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
rs7978540
×
Entrez Id:
23085
Gene Symbol:
ERC1
ERC1
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
rs61740169
×
Entrez Id:
23085
Gene Symbol:
ERC1
ERC1
Complete hydatidiform mole
0.010
GeneticVariation
BEFREE
Two single nucleotide polymorphisms, c.G48C(p.Q16H ) in<i>ERC1</i> and c.G1114A(p.G372S) in <i>KCNG4</i>, were associated with an increased risk of CHM (<i>p</i><0.05).
29088863
2017