List of variants in gene combination LOC126806423, TTN reported as likely benign for TTN-related disorder

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.68007G>A (p.Lys22669=)	rs755897447	0.00004
NM_001267550.2(TTN):c.67444C>T (p.Arg22482Trp)	rs563233842	0.00002
NM_001267550.2(TTN):c.67809G>A (p.Ala22603=)	rs548223512	0.00002

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