List of variants in gene combination LOC126806429, TTN reported as benign for autosomal recessive disease

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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: 8

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HGVS	dbSNP	gnomAD frequency
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.19738C>T (p.Pro6580Ser)	rs116572520	0.00188
NM_001267550.2(TTN):c.20175A>G (p.Ile6725Met)	rs146627500	0.00104
NM_001267550.2(TTN):c.20236G>A (p.Ala6746Thr)	rs202108224	0.00081
NM_001267550.2(TTN):c.20025C>A (p.Ala6675=)	rs373842558	0.00079
NM_001267550.2(TTN):c.19818A>G (p.Lys6606=)	rs397517492	0.00003
NM_001267550.2(TTN):c.20142C>T (p.Tyr6714=)	rs535793314

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