FNIP1, folliculin interacting protein 1, 96459

N. diseases: 24; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs79577858
rs79577858
Entrez Id: 96459
Gene Symbol: FNIP1
FNIP1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs593767
rs593767
Entrez Id: 96459
Gene Symbol: FNIP1
FNIP1
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: rs26008
rs26008
Entrez Id: 96459
Gene Symbol: FNIP1
FNIP1
CUI: C0202236
Disease:
Triglycerides measurement 		C 0.700 GeneticVariation GWASCAT Exome-wide association study of plasma lipids in >300,000 individuals. 29083408 2017
dbSNP: rs185120612
rs185120612
Entrez Id: 96459
Gene Symbol: FNIP1
FNIP1
CUI: C0200641
Disease:
Blood basophil count (lab test) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs185120612
rs185120612
Entrez Id: 96459
Gene Symbol: FNIP1
FNIP1
CUI: C0200638
Disease:
Eosinophil count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs758324
rs758324
Entrez Id: 96459
Gene Symbol: FNIP1
FNIP1
CUI: C0002395
Disease:
Alzheimer's Disease 		T 0.700 GeneticVariation GWASCAT A novel Alzheimer disease locus located near the gene encoding tau protein. 25778476 2016