rs114807680
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Adenocarcinoma of lung (disorder)
A
0.700
GeneticVariation
GWASCAT
Genome-wide association study of familial lung cancer.
29924316
2018
rs9851441
EPHB1;CEP63
Body Height
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs10935143
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Body mass index
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs62270313
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Epilepsy
0.700
GeneticVariation
GWASCAT
GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy.
26220383
2015
rs1338928289
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Gastric Adenocarcinoma
0.700
GeneticVariation
UNIPROT
rs183252871
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Iron binding capacity total measurement
T
0.700
GeneticVariation
GWASCAT
Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?
28334935
2017
rs187472012
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Iron binding capacity total measurement
A
0.700
GeneticVariation
GWASCAT
Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?
28334935
2017
rs6766459
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Liver carcinoma
0.010
GeneticVariation
BEFREE
Five polymorphisms (rs11929692, rs7644369, rs6776570, rs3821502, and rs6766459 ) of the EPHB1 gene and alleles of 2 polymorphisms (rs1502174 and rs9877457) were associated with HCC (p < 0.05 for both).
21763378
2011
rs62270313
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Maculopapular Lesion
0.700
GeneticVariation
GWASCAT
GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy.
26220383
2015
rs377332009
EPHB1;CEP63;KY
MYOPATHY, MYOFIBRILLAR, 7
T
0.700
CausalMutation
CLINVAR
rs886037917
EPHB1;CEP63;KY
MYOPATHY, MYOFIBRILLAR, 7
T
0.700
CausalMutation
CLINVAR
rs16842236
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Narcolepsy
0.700
GeneticVariation
GWASDB
Genome-wide association database developed in the Japanese Integrated Database Project.
19629137
2009
rs966513
EPHB1;LOC102724019
Papillary thyroid carcinoma
0.010
GeneticVariation
BEFREE
In a multicenter retrospective case-control study, five thyroid cancer-related SNPs-rs966513 (9q22.33, FOXE1), rs944289 (14q13.3, PTCSC3), rs2439302 (8p12, NRG1), rs1867277 (9q22.23, FOXE1), and rs6983267 (8q24, POU5F1B)-were genotyped in 959 cases of histologically verified FA, 535 papillary thyroid carcinomas (PTC), and 2766 population controls.
25562676
2015
rs1085307110
EPHB1;CEP63;KY
Paraparesis, Spastic
CATGTCGATAGATACAGCACATGTCGATA
0.700
CausalMutation
CLINVAR
Progressive hereditary spastic paraplegia caused by a homozygous KY mutation.
28488683
2017
rs2030737
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Parkinson Disease
0.010
GeneticVariation
BEFREE
The DCC rs17468382 and EPHB1 rs2030737 SNPs may be associated with increased PD risk, and the CHP rs6492998 and RRAS2 rs2970332 SNPs may be associated with reduced PD risk.
21085126
2011
rs11918092
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Schizophrenia
0.010
GeneticVariation
BEFREE
Association of EPHB1 rs11918092 and EFNB2 rs9520087 with psychopathological symptoms of schizophrenia in Chinese Zhuang and Han populations.
27028544
2016
rs11918092
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Secondary malignant neoplasm of colon and/or rectum
C
0.700
GeneticVariation
GWASCAT
A genome-wide association study identifies single nucleotide polymorphisms associated with time-to-metastasis in colorectal cancer.
30738427
2019
rs1085307110
EPHB1;CEP63;KY
Spastic Paraplegia
CATGTCGATAGATACAGCACATGTCGATA
0.700
CausalMutation
CLINVAR
Progressive hereditary spastic paraplegia caused by a homozygous KY mutation.
28488683
2017
rs1085307110
EPHB1;CEP63;KY
Spastic Paraplegia, Hereditary
CATGTCGATAGATACAGCACATGTCGATA
0.700
CausalMutation
CLINVAR
Progressive hereditary spastic paraplegia caused by a homozygous KY mutation.
28488683
2017
rs183252871
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Total iron binding capacity function
T
0.700
GeneticVariation
GWASCAT
Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?
28334935
2017
rs187472012
×
Entrez Id:
2047
Gene Symbol:
EPHB1
EPHB1
Total iron binding capacity function
A
0.700
GeneticVariation
GWASCAT
Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?
28334935
2017
rs6775611
EPHB1;CEP63;KY
Vital capacity
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs775009958
EPHB1;CEP63
Waist-Hip Ratio
T
0.700
GeneticVariation
GWASCAT
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.
28552196
2017