rs1217691063, MTHFR

N. diseases: 614
Disease: Acrocyanosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Acrocyanosis
CUI: C0221347
Disease: Acrocyanosis
0.010 GeneticVariation BEFREE The risk of acrocyanosis was significantly higher in patients homozygous for the mutation c.677C>T compared to those with no mutation (OR = 4.8 (95%CI 1.5-14.9)). 23816603 2015