GPR19, G protein-coupled receptor 19, 2842

N. diseases: 12; N. variants: 24
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10845606
rs10845606
Entrez Id: 2842
Gene Symbol: GPR19
GPR19
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		C 0.800 GeneticVariation GWASCAT Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. 23273568 2013
dbSNP: rs10845606
rs10845606
Entrez Id: 2842
Gene Symbol: GPR19
GPR19
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		C 0.800 GeneticVariation GWASDB Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. 23273568 2013
dbSNP: rs34330
rs34330
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		C 0.800 GeneticVariation GWASDB Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. 23273568 2013
dbSNP: rs34330
rs34330
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		C 0.800 GeneticVariation GWASCAT Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. 23273568 2013
dbSNP: rs2066827
rs2066827
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C0600139
Disease:
Prostate carcinoma 		0.730 GeneticVariation BEFREE Our present study showed evidence that CDKN1B Val 109 Gly variant is not related to PCa risk. 31257659 2019
dbSNP: rs2066827
rs2066827
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C0600139
Disease:
Prostate carcinoma 		T 0.730 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016 2018
dbSNP: rs2066827
rs2066827
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C0600139
Disease:
Prostate carcinoma 		0.730 GeneticVariation BEFREE Further large-scale studies are needed to clarify the role of CDKN1B V109G polymorphism on prostate cancer risk. 18645269 2008
dbSNP: rs2066827
rs2066827
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C0600139
Disease:
Prostate carcinoma 		0.730 GeneticVariation BEFREE In addition, a case-control study has shown that the 326T/G (V109G) polymorphism in CDKN1B is associated with advanced prostate cancer. 15026335 2004
dbSNP: rs111909987
rs111909987
Entrez Id: 2842
Gene Symbol: GPR19
GPR19
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs35756741
rs35756741
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7969505
rs7969505
Entrez Id: 2842
Gene Symbol: GPR19
GPR19
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs719839
rs719839
Entrez Id: 2842
Gene Symbol: GPR19
GPR19
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs7486387
rs7486387
Entrez Id: 2842
Gene Symbol: GPR19
GPR19
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs7311556
rs7311556
Entrez Id: 2842
Gene Symbol: GPR19
GPR19
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs7311556
rs7311556
Entrez Id: 2842
Gene Symbol: GPR19
GPR19
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs1060500186
rs1060500186
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C1970712
Disease:
Multiple Endocrine Neoplasia, Type IV 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121917832
rs121917832
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C1970712
Disease:
Multiple Endocrine Neoplasia, Type IV 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1555085575
rs1555085575
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C1970712
Disease:
Multiple Endocrine Neoplasia, Type IV 		GC 0.700 CausalMutation CLINVAR
dbSNP: rs532903617
rs532903617
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C1970712
Disease:
Multiple Endocrine Neoplasia, Type IV 		G 0.700 CausalMutation CLINVAR
dbSNP: rs551236750
rs551236750
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C0221002
Disease:
Hyperparathyroidism, Primary 		T 0.700 CausalMutation CLINVAR
dbSNP: rs774454456
rs774454456
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C1970712
Disease:
Multiple Endocrine Neoplasia, Type IV 		C 0.700 CausalMutation CLINVAR
dbSNP: rs774454456
rs774454456
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C0221002
Disease:
Hyperparathyroidism, Primary 		C 0.700 CausalMutation CLINVAR
dbSNP: rs777354267
rs777354267
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C1970712
Disease:
Multiple Endocrine Neoplasia, Type IV 		T 0.700 CausalMutation CLINVAR
dbSNP: rs786201007
rs786201007
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C1970712
Disease:
Multiple Endocrine Neoplasia, Type IV 		GCAGGCGGAGCACCCCAAGC 0.700 CausalMutation CLINVAR
dbSNP: rs786201010
rs786201010
Entrez Id: 1027;2842
Gene Symbol: CDKN1B;GPR19
CDKN1B;GPR19
CUI: C1970712
Disease:
Multiple Endocrine Neoplasia, Type IV 		C 0.700 CausalMutation CLINVAR