RGS7, regulator of G protein signaling 7, 6000

N. diseases: 28; N. variants: 25
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs116135446
rs116135446
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs146390073
rs146390073
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
CUI: C1531624
Disease:
Cardioembolic stroke 		0.700 GeneticVariation GWASCAT Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. 29531354 2018
dbSNP: rs10802916
rs10802916
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs10926380
rs10926380
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs11586002
rs11586002
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs12038552
rs12038552
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs12038552
rs12038552
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs12119557
rs12119557
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs16841100
rs16841100
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs16841101
rs16841101
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs16841106
rs16841106
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
CUI: C0023467
Disease:
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
dbSNP: rs16841107
rs16841107
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs1915872
rs1915872
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
CUI: C0428883
Disease:
Diastolic blood pressure 		0.700 GeneticVariation GWASCAT EPHA6 rs4857055 C > T polymorphism associates with hypertension through triglyceride and LDL particle size in the Korean population. 29208002 2017
dbSNP: rs1996806
rs1996806
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs2502439
rs2502439
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
CUI: C0023467
Disease:
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
dbSNP: rs2616968
rs2616968
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs4659585
rs4659585
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs4659586
rs4659586
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs4660051
rs4660051
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs4660051
rs4660051
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs6682594
rs6682594
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs6690744
rs6690744
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
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: rs679992
rs679992
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes. 25102180 2014
dbSNP: rs16840647
rs16840647
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
CUI: C0022336
Disease:
Creutzfeldt-Jakob disease 		0.700 GeneticVariation GWASDB Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk. 22137330 2012
dbSNP: rs746273282
rs746273282
Entrez Id: 6000
Gene Symbol: RGS7
RGS7
CUI: C0025202
Disease:
melanoma 		0.010 GeneticVariation BEFREE RGS7 was mutated in 11% of melanomas and was found to harbor three recurrent mutations (p.R44C, p.E383K and p.R416Q). 29330521 2018