List of variants in gene combination LOC126806426, TTN reported as uncertain significance for Myopathy, myofibrillar, 9, with early respiratory failure

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.49070C>T (p.Ala16357Val)	rs199768159	0.00009
NM_001267550.2(TTN):c.48671G>C (p.Trp16224Ser)	rs886055270
NM_001267550.2(TTN):c.48760+8T>C	rs2057012531
NM_001267550.2(TTN):c.49183A>G (p.Ser16395Gly)	rs2056873203
NM_001267550.2(TTN):c.49211C>T (p.Thr16404Ile)	rs2056867382
NM_001267550.2(TTN):c.49265T>C (p.Ile16422Thr)	rs746167353

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