Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs781902168
rs781902168
CRYAB ; HSPB2 ; HSPB2-C11orf52
0.010 GeneticVariation BEFREE Subsequent interrogation of our entire cohort of familial cases identified a second familial case localized to chromosome 11q23 harboring a c.31C>T (p.R11C) mutation. 26402864

2015