List of variants in gene TTR reported as benign for amyloidosis

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.337-18G>C	rs36204272	0.06198
NM_000371.4(TTR):c.76G>A (p.Gly26Ser)	rs1800458	0.05309
NM_000371.4(TTR):c.*21C>A	rs12226	0.02158
NM_000371.3(TTR):c.*345G>A	rs58172837	0.01182
NM_000371.4(TTR):c.336+19G>A	rs75517067	0.00309
NM_000371.4(TTR):c.416C>T (p.Thr139Met)	rs28933981	0.00177
NM_000371.4(TTR):c.360C>T (p.Ser120=)	rs150127220	0.00128
NM_000371.4(TTR):c.417G>A (p.Thr139=)	rs2276382	0.00104
NM_000371.4(TTR):c.328C>A (p.His110Asn)	rs121918074	0.00040
NM_000371.3(TTR):c.*191C>T	rs556327750	0.00023
NM_000371.4(TTR):c.371G>A (p.Arg124His)	rs121918095	0.00019
NM_000371.4(TTR):c.-743A>T	rs3794885
NM_000371.4(TTR):c.337-14_337-11del	rs112263266
NM_000371.4(TTR):c.372C>G (p.Arg124=)	rs780119793
NM_000371.4(TTR):c.70-7C>T	rs587780990

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