ISL1, ISL LIM homeobox 1, 3670

N. diseases: 94; N. variants: 2
Disease: Coronary heart disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1017
rs1017
Entrez Id: 3670
Gene Symbol: ISL1
ISL1
CUI: C0010068
Disease:
Coronary heart disease 		0.030 GeneticVariation BEFREE We concluded that rs1017 contributed to the risk of CHD in Chinese Han people, and ISL1 may be involved in the formation and development of the heart. 24634231 2014
dbSNP: rs1017
rs1017
Entrez Id: 3670
Gene Symbol: ISL1
ISL1
CUI: C0010068
Disease:
Coronary heart disease 		0.030 GeneticVariation BEFREE In conclusion, ISL1 common variant rs1017 is not associated with increased genetic risk of CHD in the white population. 23229290 2013
dbSNP: rs1017
rs1017
Entrez Id: 3670
Gene Symbol: ISL1
ISL1
CUI: C0010068
Disease:
Coronary heart disease 		0.030 GeneticVariation BEFREE This is the first study which indicates that ISL1 common variant rs1017 may not play a role in sporadic CHD susceptibility in the Chinese population. 22480195 2012