Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121964857
rs121964857
TNNT2
0.710 GeneticVariation BEFREE TNNT2 R278C was present in a woman with severe HC, but a sister and a daughter were mutation carriers and did not have hypertrophy. 12881443

2003
dbSNP: rs121964857
rs121964857
TNNT2
A 0.710 GeneticVariation CLINVAR