Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11895772
rs11895772
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C0021704
Disease:
Intelligence
C 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs4851284
rs4851284
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C0205682
Disease:
Waist-Hip Ratio
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs6542924
rs6542924
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs71413877
rs71413877
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs75152355
rs75152355
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C0021704
Disease:
Intelligence
T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs7582180
rs7582180
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs10183150
rs10183150
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
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: rs4851287
rs4851287
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C1305855
Disease:
Body mass index
A 0.700 GeneticVariation GWASCAT Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. 29273807 2018
dbSNP: rs71413877
rs71413877
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
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: rs71413877
rs71413877
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs71413877
rs71413877
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs7606277
rs7606277
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C0021704
Disease:
Intelligence
A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs773205136
rs773205136
Entrez Id: 164832
Gene Symbol: LONRF2
LONRF2
CUI: C0009402
Disease:
Colorectal Carcinoma
0.700 GeneticVariation UNIPROT