Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800470
rs1800470
TGFB1
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.010 GeneticVariation BEFREE The previously reported association of the coding SNP rs1800470 with high myopia was successfully replicated. 19365037

2009