Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4651005
rs4651005
Entrez Id: 55103
Gene Symbol: RALGPS2
RALGPS2
CUI: C0016529
Disease:
Forced expiratory volume function
T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs4651005
rs4651005
Entrez Id: 55103
Gene Symbol: RALGPS2
RALGPS2
CUI: C0042834
Disease:
Vital capacity
T 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs6425501
rs6425501
Entrez Id: 55103
Gene Symbol: RALGPS2
RALGPS2
CUI: C0042834
Disease:
Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2184464
rs2184464
Entrez Id: 55103
Gene Symbol: RALGPS2
RALGPS2
CUI: C2985280
Disease:
Blood Protein Measurement
G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs2297687
rs2297687
Entrez Id: 9068;55103
Gene Symbol: ANGPTL1;RALGPS2
ANGPTL1;RALGPS2
CUI: C0202236
Disease:
Triglycerides measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs1292187704
rs1292187704
Entrez Id: 9068;55103
Gene Symbol: ANGPTL1;RALGPS2
ANGPTL1;RALGPS2
CUI: C0752123
Disease:
Spinocerebellar Ataxia Type 5
0.010 GeneticVariation BEFREE Beta-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi. 20603325 2010