List of variants in gene TTN reported as likely pathogenic by New York Genome Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.54418C>T (p.Arg18140Ter)	rs747236787	0.00001
NM_001267550.2(TTN):c.55660C>T (p.Arg18554Ter)	rs1483931960	0.00001
NM_001267550.2(TTN):c.67348+1G>A	rs758279518	0.00001
NM_001267550.2(TTN):c.69420del (p.Gly23141fs)	rs1330960948	0.00001
NM_001267550.2(TTN):c.94855C>T (p.Arg31619Ter)	rs869312121	0.00001
NM_001267550.2(TTN):c.66753T>G (p.Tyr22251Ter)	rs2047743679
NM_001267550.2(TTN):c.89993C>A (p.Ser29998Ter)	rs376543931
NM_001267550.2(TTN):c.98810_98811del (p.Lys32937fs)

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