ClinVar for PubMed (Select 31074293) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1075407	NM_000371.4(TTR):c.94C>G (p.Leu32Val)	TTR (L32V)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GPathogenic
Select item 1066429	NM_000371.4(TTR):c.179C>A (p.Thr60Asn)	TTR (T60N)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GPathogenic/Likely pathogenic