Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs150766139
rs150766139
Entrez Id: 4913;7249
Gene Symbol: NTHL1;TSC2
NTHL1;TSC2
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
A 0.700 CausalMutation CLINVAR