Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1312268347
rs1312268347
SARDH
0.010 GeneticVariation BEFREE For <i>SDHC</i>, <i>c.380A>G</i> presented in 48 RCC patients, and for <i>SDHA</i> a novel germline mutation c.2T>C: p.M1T in an occasional case of gastrointestinal stromal tumor intricate with RCC. 31579262

2019