Gene: TGFBR3L ×
Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11669203
rs11669203
MAP2K7 ; TGFBR3L
0.010 GeneticVariation 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