List of variants in gene TTR reported as likely pathogenic by Stanford Center for Inherited Cardiovascular Disease, Stanford University

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_000371.4(TTR):c.130C>T (p.Pro44Ser)	rs11541790	0.00001
NM_000371.4(TTR):c.238A>G (p.Thr80Ala)	rs121918070	0.00001
NM_000371.4(TTR):c.407A>C (p.Tyr136Ser)	rs730881167

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