List of variants in gene combination LOC126806421, TTN reported as uncertain significance for Primary dilated cardiomyopathy

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

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.96235G>A (p.Asp32079Asn)	rs200540781
NM_001267550.2(TTN):c.96613G>A (p.Val32205Met)	rs372312129
NM_001267550.2(TTN):c.96892C>T (p.Gln32298Ter)	rs201108270

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