Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
MTHFR
0.010 GeneticVariation BEFREE The presence of MTHFR C677T mutation influences the incidence of macrovascular abnormalities in SSc patients. 19093229

2009