List of variants in gene TTN reported as likely pathogenic by Undiagnosed Diseases Network, NIH

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.16054G>A (p.Asp5352Asn)	rs1190242728	0.00001
NM_001267550.2(TTN):c.102956_102958del (p.Thr34319del)	rs878854378
NM_001267550.2(TTN):c.44516del (p.Asp14839fs)	rs2058865334

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