Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4837628
rs4837628
Entrez Id: 1620
Gene Symbol: BRINP1
BRINP1
CUI: C0030567
Disease:
Parkinson Disease 		A 0.800 GeneticVariation GWASCAT Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850 2010
dbSNP: rs4837628
rs4837628
Entrez Id: 1620
Gene Symbol: BRINP1
BRINP1
CUI: C0030567
Disease:
Parkinson Disease 		A 0.800 GeneticVariation GWASDB Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. 20070850 2010
dbSNP: rs4837631
rs4837631
Entrez Id: 1620
Gene Symbol: BRINP1
BRINP1
CUI: C0037369
Disease:
Smoking 		T 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
dbSNP: rs28503451
rs28503451
Entrez Id: 1620
Gene Symbol: BRINP1
BRINP1
CUI: C0596887
Disease:
mathematical ability 		T 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: rs748525584
rs748525584
Entrez Id: 1620
Gene Symbol: BRINP1
BRINP1
CUI: C0562350
Disease:
Hip circumference 		T 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs10984447
rs10984447
Entrez Id: 1620
Gene Symbol: BRINP1
BRINP1
CUI: C0026769
Disease:
Multiple Sclerosis 		0.010 GeneticVariation BEFREE Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease. 22492128 2012