List of variants in gene combination LOC126806428, TTN reported as 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.21106G>A (p.Asp7036Asn)	rs72648962	0.01586
NM_001267550.2(TTN):c.21044C>T (p.Ala7015Val)	rs72648960	0.00893
NM_001267550.2(TTN):c.21019A>T (p.Ile7007Phe)	rs114626713	0.00491
NM_001267550.2(TTN):c.21364G>A (p.Ala7122Thr)	rs201394117	0.00042
NM_001267550.2(TTN):c.21148C>T (p.Leu7050=)	rs202089818	0.00038
NM_001267550.2(TTN):c.20891C>T (p.Thr6964Met)	rs765257439	0.00001

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