rs377522479, ARHGAP24

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neoplasms
CUI: C0027651
Disease: Neoplasms
0.010 GeneticVariation BEFREE We also detected a very strong association between a C91T polymorphism and MYCN copy number in this tumor. 10601564 2000