Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs373356672
rs373356672
NEIL1 ; MIR631
CUI: C0022578
Disease: Keratoconus
Keratoconus 		0.010 GeneticVariation BEFREE Also, the C/T and T as well as C/C genotypes and alleles of the c.580C>T polymorphism of the same gene displayed relationship with KC occurrence. 25356504

2014