rs121913483, FGFR3

N. diseases: 22
Disease: Hypochondroplasia (disorder) ×
Source: CLINVAR ×
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypochondroplasia (disorder)
CUI: C0410529
Disease: Hypochondroplasia (disorder)
0.700 CausalMutation CLINVAR