Gene: TGFBR3L ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 100507588
Gene Symbol: TGFBR3L
TGFBR3L 		0.010 GeneticVariation disease BEFREE The SNP rs11669203 located at the MYCN binding site of TGFBR3L is significantly associated with elevated risk of NB, and abnormal MYCN-regulated TGFBR3L expression may contribute to NB oncogenesis. 26468016 2016