Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3741414
rs3741414
INHBC
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		T 0.800 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs3741414
rs3741414
INHBC
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.800 GeneticVariation GWASCAT 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. 28452372

2017
dbSNP: rs145048495
rs145048495
INHBC
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443

2018
dbSNP: rs2229357
rs2229357
INHBC
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		G 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
dbSNP: rs2229357
rs2229357
INHBC
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		G 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
dbSNP: rs3741414
rs3741414
INHBC
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		T 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals. 30993211

2019
dbSNP: rs3741414
rs3741414
INHBC
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		C 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
dbSNP: rs3741414
rs3741414
INHBC
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		C 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
dbSNP: rs3741414
rs3741414
INHBC
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 GeneticVariation GWASCAT 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. 28452372

2017
dbSNP: rs3741414
rs3741414
INHBC
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486

2013
dbSNP: rs61352607
rs61352607
INHBC
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		G 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
dbSNP: rs61352607
rs61352607
INHBC
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		G 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422

2018
dbSNP: rs61352607
rs61352607
INHBC
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		G 0.700 GeneticVariation GWASCAT The impact of low-frequency and rare variants on lipid levels. 25961943

2015
dbSNP: rs73119306
rs73119306
INHBC
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		A 0.700 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528

2019