List of variants in gene APOA1 reported as likely benign 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000039.3(APOA1):c.284T>A (p.Phe95Tyr)	rs138407155	0.00044
NM_000039.3(APOA1):c.315C>T (p.Gly105=)	rs148950234	0.00032
NM_000039.3(APOA1):c.555G>C (p.Thr185=)	rs143182884	0.00023
NM_000039.3(APOA1):c.*17C>T	rs370532459	0.00014
NM_000039.3(APOA1):c.200+19G>A	rs377408912	0.00013
NM_000039.3(APOA1):c.726G>C (p.Leu242=)	rs567268961	0.00013
NM_000039.3(APOA1):c.454G>A (p.Glu152Lys)	rs574061789	0.00010
NM_000039.3(APOA1):c.-11G>A	rs199729971	0.00005
NM_000039.3(APOA1):c.498C>A (p.Ser166Arg)	rs757899657	0.00004
NM_000039.3(APOA1):c.483G>C (p.Leu161=)	rs747245248	0.00003
NM_000039.3(APOA1):c.126C>T (p.Tyr42=)	rs1591331259	0.00001
NM_000039.3(APOA1):c.127G>C (p.Val43Leu)	rs373545875
NM_000039.3(APOA1):c.162G>C (p.Val54=)	rs193922099

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