ClinVar Miner

List of variants in gene TTR reported as likely benign for not specified

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
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.14G>A (p.Arg5His) rs138657343 0.00017
NM_000371.4(TTR):c.384C>T (p.Ala128=) rs143906738 0.00015
NM_000371.4(TTR):c.354C>T (p.Asn118=) rs11541797 0.00009
NM_000371.4(TTR):c.375C>T (p.Tyr125=) rs749079577 0.00004
NM_000371.4(TTR):c.70-20C>T rs773578107 0.00003
NM_000371.4(TTR):c.439G>T (p.Glu147Ter) rs730881162 0.00002
NM_000371.4(TTR):c.78T>C (p.Gly26=) rs779457244 0.00002
NM_000371.4(TTR):c.147C>T (p.Ala49=) rs11081703 0.00001
NM_000371.4(TTR):c.337-13T>C rs762691667 0.00001
NM_000371.3(TTR):c.-46C>T rs750577317
NM_000371.4(TTR):c.*9TCC[1] rs766223850
NM_000371.4(TTR):c.201-27C>A rs1315540051
NM_000371.4(TTR):c.216T>G (p.Ser72=) rs1555631392
NM_000371.4(TTR):c.231G>A (p.Gly77=) rs1555631396
NM_000371.4(TTR):c.303A>C (p.Ala101=) rs1555631418
NM_000371.4(TTR):c.369C>G (p.Arg123=) rs1598846734
NM_000371.4(TTR):c.69+7G>A rs1453023289
NM_000371.4(TTR):c.70-19G>A rs548935944

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