rs80338844, SDHD

N. diseases: 10
Disease: Neoplasms ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neoplasms
CUI: C0027651
Disease: Neoplasms
0.010 GeneticVariation BEFREE In addition to tumour type susceptibility differences for individual genes, we confirmed that the <i>SDHD:</i>p.Pro81Leu mutation has a distinct phenotype and identified increased age-related tumour risks with highly destabilising <i>SDHB</i> missense mutations. 29386252 2018