Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200397144
rs200397144
SDHA
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 GeneticVariation BEFREE Another tumor (from France) carried a germline SDHA missense mutation c.1753C → T (p.Arg585Trp). 21752896

2011