List of variants in gene combination LOC126806422, TTN reported as likely benign 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.70506G>T (p.Gly23502=)	rs181702963	0.00007
NM_001267550.2(TTN):c.70305G>A (p.Thr23435=)	rs397517684	0.00006
NM_001267550.2(TTN):c.70331C>G (p.Pro23444Arg)	rs1325284144	0.00001
NM_001267550.2(TTN):c.69604A>G (p.Thr23202Ala)
NM_001267550.2(TTN):c.69806G>A (p.Gly23269Glu)
NM_001267550.2(TTN):c.69876A>G (p.Thr23292=)	rs1267766480

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