rs1318358361, ARID1B

N. diseases: 13
Disease: Sudden infant death syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Sudden infant death syndrome
CUI: C0038644
Disease: Sudden infant death syndrome
0.010 GeneticVariation BEFREE Sudden infant death in a patient with FGFR3 P250R mutation. 17103449 2006