rs7229639, SMAD7

N. diseases: 13
Disease: Familial (FPAH) ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
0.010 GeneticVariation BEFREE SNPs rs7229639 and rs4939827 explained approximately 1% of the familial relative risk of CRC in East Asians. 24448986 2014