List of variants in gene APOA1 reported as uncertain significance for familial visceral 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_000039.3(APOA1):c.80C>A (p.Pro27His)	rs121912720	0.00007
NM_000039.3(APOA1):c.-29G>A	rs1430134542	0.00002
NM_000039.3(APOA1):c.127G>A (p.Val43Met)	rs373545875	0.00002
NM_000039.3(APOA1):c.168G>A (p.Gln56=)	rs760886281	0.00002
NM_000039.3(APOA1):c.41C>T (p.Thr14Met)	rs778560581	0.00002
NM_000039.3(APOA1):c.101G>T (p.Arg34Leu)	rs28929476	0.00001
NM_000039.3(APOA1):c.116C>T (p.Ala39Val)	rs746314593	0.00001
NM_000039.3(APOA1):c.379G>A (p.Asp127Asn)	rs921646982	0.00001
NM_000039.3(APOA1):c.271G>T (p.Val91Leu)	rs2134231457
NM_000039.3(APOA1):c.388AAG[1] (p.Lys131del)	rs532489785
NM_000039.3(APOA1):c.447G>A (p.Glu149=)	rs1941542293
NM_000039.3(APOA1):c.480G>T (p.Glu160Asp)	rs769548576
NM_000039.3(APOA1):c.664G>A (p.Glu222Lys)	rs121912717
NM_000039.3(APOA1):c.677C>T (p.Thr226Met)	rs1941530805
NM_000039.3(APOA1):c.705C>G (p.Leu235=)	rs1941529555

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