Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs727504245
rs727504245
TNNT2
0.710 GeneticVariation BEFREE We have identified a novel missense mutation in exon 9 (Ala104Val) of the cTnT gene in a patient with familial HCM. 9140840

1997
dbSNP: rs727504245
rs727504245
TNNT2
A 0.710 GeneticVariation CLINVAR