List of variants in gene TTN reported as uncertain significance for SUDDEN INFANT DEATH SYNDROME

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.64898G>A (p.Arg21633Gln)	rs141965360	0.00016
NM_001267550.2(TTN):c.43622C>T (p.Ser14541Leu)	rs768180052	0.00001
NM_001267550.2(TTN):c.91721A>T (p.Glu30574Val)	rs1308285808

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