rs36053993, MUTYH

N. diseases: 31
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 Our results suggest that p.(Gly396Asp) in <i>MUTYH</i>, and potentially other mutations in additional members of the same DNA excision-repair pathway (such as the <i>OGG1</i> gene) might be involved in driving the tumorigenesis leading to familial and sporadic SI-NETs. 28634180 2017