rs397507444, MTHFR

N. diseases: 306
Disease: Huntington Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
0.010 GeneticVariation BEFREE Hyperhomocysteinemia, serum folate levels and both C677T and A1298C MTHFR mutations are associated with CVD in HD patients. 12187094 2002