List of variants in gene combination LOC126806428, TTN reported as uncertain significance for 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.21103G>A (p.Val7035Ile)	rs1553913782	0.00001
NM_001267550.2(TTN):c.21277A>G (p.Thr7093Ala)	rs773883340	0.00001
NM_001267550.2(TTN):c.20905T>A (p.Cys6969Ser)	rs368762020
NM_001267550.2(TTN):c.21143G>T (p.Arg7048Leu)	rs148072021

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