Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs515726184
rs515726184
RRM2B
CUI: C0264162
Disease: Camptocormia
Camptocormia 		T 0.700 CausalMutation CLINVAR

dbSNP: rs61752783
rs61752783
POLG ; MIR6766
CUI: C0264162
Disease: Camptocormia
Camptocormia 		A 0.700 CausalMutation CLINVAR