rs587784379, RYR1

N. diseases: 2
Disease: Arthrogryposis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Arthrogryposis
CUI: C0003886
Disease: Arthrogryposis
0.700 CausalMutation CLINVAR The genomic and clinical landscape of fetal akinesia. 31680123 2020