List of variants in gene combination LOC126806425, TTN reported as likely pathogenic for not provided

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.52553G>A (p.Arg17518His)	rs559590585	0.00001
NM_001267550.2(TTN):c.52694_52695del (p.His17565fs)
NM_001267550.2(TTN):c.52903C>T (p.Arg17635Ter)	rs2154197219
NM_001267550.2(TTN):c.52999C>T (p.Gln17667Ter)	rs794729272
NM_001267550.2(TTN):c.53206C>T (p.Arg17736Ter)	rs571702144
NM_001267550.2(TTN):c.53259del (p.Lys17753fs)	rs1389777522
NM_001267550.2(TTN):c.53287+1G>T	rs1064794266

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