Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs497078
rs497078
0.020 GeneticVariation BEFREE Our study provides evidence that CTRC variants, including c.180TT (p.Gly60Gly) are strong CP risk factors. 28968289

2017

dbSNP: rs497078
rs497078
0.020 GeneticVariation BEFREE The authors also observed significant association for the synonymous variant c.180C>T (p.(=)) with CP (OR 2.71, 95% CI 1.79 to 4.12, p=5.3 × 10(-7)). 22580415

2013