List of variants in gene combination LOC126806429, TTN reported as benign for not provided

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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.19994-63T>C	rs2255480	0.02404
NM_001267550.2(TTN):c.19976C>T (p.Thr6659Met)	rs16866475	0.01294
NM_001267550.2(TTN):c.20147T>A (p.Met6716Lys)	rs28626194	0.00641
NM_001267550.2(TTN):c.20175A>G (p.Ile6725Met)	rs146627500	0.00104

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