Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4074995
rs4074995
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C2239219
Disease:
von Willebrand's factor (lab test) 		0.700 GeneticVariation GWASDB Ischemic stroke is associated with the ABO locus: the EuroCLOT study. 23381943 2013
dbSNP: rs4074995
rs4074995
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0202159
Disease:
Parathyroid hormone measurement 		G 0.700 GeneticVariation GWASCAT The other SNPs associated with serum PTH concentration included rs4074995 within <i>RGS14</i> (<i>P</i>=6.6 × 10<sup>-17</sup>), rs219779 adjacent to <i>CLDN14</i> (<i>P</i>=3.5 × 10<sup>-16</sup>), rs4443100 near <i>RTDR1</i> (<i>P</i>=8.7 × 10<sup>-9</sup>), and rs73186030 near <i>CASR</i> (<i>P</i>=4.8 × 10<sup>-8</sup>). 27927781 2017
dbSNP: rs4074995
rs4074995
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0523827
Disease:
Inorganic phosphate measurement 		0.700 GeneticVariation GWASDB Common genetic variants associate with serum phosphorus concentration. 20558539 2010
dbSNP: rs4075958
rs4075958
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.800 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs4075958
rs4075958
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.800 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088 2011
dbSNP: rs4075958
rs4075958
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C2239219
Disease:
von Willebrand's factor (lab test) 		0.700 GeneticVariation GWASDB Ischemic stroke is associated with the ABO locus: the EuroCLOT study. 23381943 2013
dbSNP: rs4075958
rs4075958
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4976646
rs4976646
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0009324
Disease:
Ulcerative Colitis 		0.700 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs4976646
rs4976646
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0005845
Disease:
Blood urea nitrogen measurement 		T 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs4976646
rs4976646
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0009324
Disease:
Ulcerative Colitis 		G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs4976646
rs4976646
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs4976646
rs4976646
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0021390
Disease:
Inflammatory Bowel Diseases 		0.700 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs4976646
rs4976646
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0026769
Disease:
Multiple Sclerosis 		G 0.700 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602 2013
dbSNP: rs4976646
rs4976646
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0010346
Disease:
Crohn Disease 		G 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs4976646
rs4976646
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0022661
Disease:
Kidney Failure, Chronic 		C 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs56235845
rs56235845
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0518015
Disease:
Hemoglobin measurement 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs56235845
rs56235845
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0018935
Disease:
Hematocrit procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs6556312
rs6556312
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C2239219
Disease:
von Willebrand's factor (lab test) 		0.700 GeneticVariation GWASDB Ischemic stroke is associated with the ABO locus: the EuroCLOT study. 23381943 2013
dbSNP: rs6556313
rs6556313
Entrez Id: 10636
Gene Symbol: RGS14
RGS14
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019