Gene: MYCN ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893648
rs104893648
MYCN
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553370260
rs1553370260
MYCN ; MYCNOS
ACTCG 0.700 CausalMutation CLINVAR

dbSNP: rs1553370918
rs1553370918
MYCN
C 0.700 CausalMutation CLINVAR

dbSNP: rs367962377
rs367962377
MYCN
A 0.700 CausalMutation CLINVAR