Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs796053505
rs796053505
TSC2
CT 0.700 CausalMutation CLINVAR Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings. 29926239

2018
dbSNP: rs796053505
rs796053505
TSC2
CT 0.700 CausalMutation CLINVAR LOVD v.2.0: the next generation in gene variant databases. 21520333

2011