List of variants in gene combination LOC126806430, TTN reported as likely benign 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18470T>C (p.Ile6157Thr)	rs371882162	0.00009
NM_001267550.2(TTN):c.18549C>T (p.Asp6183=)	rs200549353	0.00002
NM_001267550.2(TTN):c.18247A>G (p.Ile6083Val)	rs374012753	0.00001
NM_001267550.2(TTN):c.18669G>A (p.Thr6223=)	rs772600691	0.00001

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