Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs45469099
rs45469099
TSC2
T 0.700 CausalMutation CLINVAR LOVD v.2.0: the next generation in gene variant databases. 21520333

2011
dbSNP: rs45469099
rs45469099
TSC2
T 0.700 CausalMutation CLINVAR Tuberous sclerosis complex consensus conference: revised clinical diagnostic criteria. 9881533

1998