RS3731746 TTN
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Associated Conditions
Early-onset myopathy with fatal cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Tibial muscular dystrophy
Dilated cardiomyopathy 1G
Myopathy
myofibrillar
9
with early respiratory failure
Early-onset myopathy with fatal cardiomyopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Tibial muscular dystrophy
Dilated cardiomyopathy 1G
Myopathy
myofibrillar
9
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Atrial fibrillation | A | β: 0.086 | 3E-91 | PubMed |
Population Frequencies
gnomAD ALL
0%
1kG AFR
34.4%
1kG ALL
65.8%
1kG AMR
79.4%
1kG EAS
62.9%
1kG EUR
17.1%
1kG SAS
31.7%
Other Variants in TTN