Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060503770
rs1060503770
SDHD
0.710 GeneticVariation BEFREE A nonsense germline heterozygous mutation (Q109X) was found in the exon 4 of the SDHD gene in the index cases of six unrelated families affected by PHEO/PGL. 17102085

2006
dbSNP: rs1060503770
rs1060503770
SDHD
T 0.710 CausalMutation CLINVAR