Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs55884799
rs55884799
Entrez Id: 3790
Gene Symbol: KCNS3
KCNS3
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs55884799
rs55884799
Entrez Id: 3790
Gene Symbol: KCNS3
KCNS3
CUI: C1518922
Disease:
peak expiratory flow (procedure) 		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: rs55884799
rs55884799
Entrez Id: 3790
Gene Symbol: KCNS3
KCNS3
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: rs55884799
rs55884799
Entrez Id: 3790
Gene Symbol: KCNS3
KCNS3
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: rs62126408
rs62126408
Entrez Id: 3790
Gene Symbol: KCNS3
KCNS3
CUI: C0016529
Disease:
Forced expiratory volume function 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. 28166213 2017
dbSNP: rs61067109
rs61067109
Entrez Id: 3790
Gene Symbol: KCNS3
KCNS3
CUI: C0016529
Disease:
Forced expiratory volume function 		G 0.700 GeneticVariation GWASCAT Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. 26635082 2015
dbSNP: rs16984239
rs16984239
Entrez Id: 3790
Gene Symbol: KCNS3
KCNS3
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis 		0.010 GeneticVariation BEFREE Our two-locus analysis showed that two two-locus combinations--rs4363506 (SNP1) and rs3733242 (SNP2), and rs4363506 and rs16984239 (SNP3) -- were significantly associated with sporadic ALS. 19740415 2009