rs2197706, None

N. diseases: 2
Disease: Fragile X Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fragile X Syndrome
CUI: C0016667
Disease: Fragile X Syndrome
0.700 GeneticVariation GWASCAT Common-variant associations with fragile X syndrome. 30531935 2019