ClinVar Miner

List of variants in gene combination LOC129935186, TTN reported as uncertain significance for Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.97192+4A>G	rs370069759	0.00001
NM_001267550.2(TTN):c.97192+5G>A	rs2154142801

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