Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28937900
rs28937900
FKRP
0.710 GeneticVariation BEFREE Patients with the C826A change had the clinically less severe LGMD2I phenotype, suggesting that this is a less disruptive FKRP mutation than those found in MDC1C. 11741828

2001
dbSNP: rs28937900
rs28937900
FKRP
A 0.710 CausalMutation CLINVAR