List of variants in gene TTN reported as likely benign for atrial fibrillation

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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.101212C>T (p.Arg33738Cys)	rs56273463	0.00613
NM_001267550.2(TTN):c.69130C>T (p.Pro23044Ser)	rs55980498	0.00372
NM_001267550.2(TTN):c.44014G>A (p.Asp14672Asn)	rs1339350914	0.00001
NM_001267550.2(TTN):c.63976C>T (p.His21326Tyr)	rs1413306492	0.00001
NM_001267550.2(TTN):c.42513T>A (p.His14171Gln)	rs142842339
NM_001267550.2(TTN):c.57356A>T (p.Lys19119Met)	rs1576219870

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