rs397514262
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
AMYOTROPHIC LATERAL SCLEROSIS 19
T
0.800
CausalMutation
CLINVAR
rs397514262
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
AMYOTROPHIC LATERAL SCLEROSIS 19
0.800
GeneticVariation
UNIPROT
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.
24119685
2013
rs397514263
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
AMYOTROPHIC LATERAL SCLEROSIS 19
A
0.800
CausalMutation
CLINVAR
rs397514263
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
AMYOTROPHIC LATERAL SCLEROSIS 19
0.800
GeneticVariation
UNIPROT
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.
24119685
2013
rs13393577
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Breast Carcinoma
T
0.710
GeneticVariation
GWASCAT
Furthermore, this study provides strong evidence implicating rs13393577 at 2q34 as a new risk variant for breast cancer .
22452962
2012
rs13393577
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Breast Carcinoma
0.710
GeneticVariation
BEFREE
Furthermore, this study provides strong evidence implicating rs13393577 at 2q34 as a new risk variant for breast cancer .
22452962
2012
rs13393577
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Malignant neoplasm of breast
0.710
GeneticVariation
BEFREE
Furthermore, this study provides strong evidence implicating rs13393577 at 2q34 as a new risk variant for breast cancer .
22452962
2012
rs13393577
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Malignant neoplasm of breast
T
0.710
GeneticVariation
GWASDB
Furthermore, this study provides strong evidence implicating rs13393577 at 2q34 as a new risk variant for breast cancer .
22452962
2012
rs1351592
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Polycystic Ovary Syndrome
G
0.710
GeneticVariation
GWASCAT
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.
26416764
2015
rs1351592
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Polycystic Ovary Syndrome
0.710
GeneticVariation
BEFREE
Genotyping analysis showed the allele frequency of rs1351592 in gene ERBB4 was significantly different (P = 1.05E-03) between PCOS cases and control group, and remained significant even after BMI adjustment (P<sub>adjusted</sub> = 2.09E-04).
28195137
2017
rs10174084
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
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
rs10207288
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
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
rs115683961
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Glycine measurement
A
0.700
GeneticVariation
GWASCAT
Assessing the causal association of glycine with risk of cardio-metabolic diseases.
30837465
2019
rs11693031
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Mood Disorders
G
0.700
GeneticVariation
GWASCAT
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.
29942085
2018
rs11693031
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Major Depressive Disorder
G
0.700
GeneticVariation
GWASCAT
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways.
29942085
2018
rs12373751
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Non-alcoholic Fatty Liver Disease
T
0.700
GeneticVariation
GWASCAT
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.
31311600
2019
rs12694277
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Systolic Pressure
T
0.700
GeneticVariation
GWASCAT
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
30224653
2018
rs13019783
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
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
rs13428799
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Triiodothyronine measurement
G
0.700
GeneticVariation
GWASCAT
Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone.
30843173
2019
rs1394780
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Thyroxine measurement
G
0.700
GeneticVariation
GWASCAT
Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone.
30843173
2019
rs1464443
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.700
GeneticVariation
GWASCAT
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
24529757
2014
rs1464443
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
0.700
GeneticVariation
GWASCAT
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
24529757
2014
rs1464443
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
AMYOTROPHIC LATERAL SCLEROSIS 1
0.700
GeneticVariation
GWASCAT
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
24529757
2014
rs1464443
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Amyotrophic Lateral Sclerosis, Sporadic
0.700
GeneticVariation
GWASCAT
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
24529757
2014
rs16825008
×
Entrez Id:
2066
Gene Symbol:
ERBB4
ERBB4
Body mass index
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019