Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555738823
rs1555738823
Entrez Id: 79147
Gene Symbol: FKRP
FKRP
CUI: C1846672
Disease:
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I
G 0.700 GeneticVariation CLINVAR FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies. 27439679 2016