Source: ALL
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
AG | 0.700 | GeneticVariation | CLINVAR | Spongious hypertrophic cardiomyopathy in patients with mutations in the four-and-a-half LIM domain 1 gene. | 22923418 | 2012 |
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|
AG | 0.700 | GeneticVariation | CLINVAR | Consequences of mutations within the C terminus of the FHL1 gene. | 19687455 | 2009 |
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|
AG | 0.700 | GeneticVariation | CLINVAR | An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1. | 18179888 | 2008 |