Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057520018
rs1057520018
Entrez Id: 6794
Gene Symbol: STK11
STK11
CUI: C4086165
Disease:
Childhood Neuroblastoma
0.010 GeneticVariation BEFREE A heterozygous missense mutation in STK11 (F354L) was identified in both the NB and FVPTC. 25751324 2015