Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886041091
rs886041091
Entrez Id: 4915
Gene Symbol: NTRK2
NTRK2
CUI: C0018552
Disease:
Hamartoma
G 0.700 GeneticVariation CLINVAR