GPR161, G protein-coupled receptor 161, 23432

N. diseases: 40; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10918822
rs10918822
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C0023467
Disease:
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
dbSNP: rs12097632
rs12097632
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C0023467
Disease:
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
dbSNP: rs12097632
rs12097632
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C0023467
Disease:
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
dbSNP: rs275137
rs275137
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C0023467
Disease:
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
dbSNP: rs275147
rs275147
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C0023467
Disease:
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
dbSNP: rs275154
rs275154
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C0023467
Disease:
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
dbSNP: rs60504827
rs60504827
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C0678222
Disease:
Breast Carcinoma 		T 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs78320035
rs78320035
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs78320035
rs78320035
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C0427460
Disease:
Red cell distribution width determination 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs10489208
rs10489208
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C0200635
Disease:
Lymphocyte Count measurement 		0.700 GeneticVariation GWASDB The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes. 22286170 2012
dbSNP: rs200635937
rs200635937
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C0349588
Disease:
Short stature 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs200635937
rs200635937
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C3714796
Disease:
Isolated somatotropin deficiency 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs200635937
rs200635937
Entrez Id: 23432
Gene Symbol: GPR161
GPR161
CUI: C4053775
Disease:
Pituitary stalk interruption syndrome 		T 0.700 GeneticVariation CLINVAR