Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs111253292
rs111253292
CORIN
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 GeneticVariation BEFREE A corin gene variant (T555I/Q568P) was identified in blacks with hypertension and cardiac hypertrophy. 22987923

2012
dbSNP: rs111253292
rs111253292
CORIN
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 GeneticVariation BEFREE The minor corin I555(P568) allele, defined by the T555I and Q568P mutations, is common in persons of African ancestry and associated with increased risk for hypertension and cardiac concentric hypertrophy. 19919978

2009
dbSNP: rs111253292
rs111253292
CORIN
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.030 GeneticVariation BEFREE We recently identified a minor allele in the corin gene defined by 2 highly linked single nucleotide polymorphisms (T555I and Q568P), which was associated with hypertension in blacks. 17296875

2007