List of variants in gene APOA1 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000039.3(APOA1):c.200+33T>C	rs2070665	0.89533
NM_000039.3(APOA1):c.43+41T>C	rs5070	0.60126
NM_000039.3(APOA1):c.732C>G (p.Pro244=)	rs5080	0.00368
NM_000039.3(APOA1):c.181G>A (p.Ala61Thr)	rs12718465	0.00091
NM_000039.3(APOA1):c.562G>T (p.Ala188Ser)	rs140770089	0.00058
NM_000039.3(APOA1):c.178T>G (p.Ser60Ala)	rs199759119	0.00043
NM_000039.3(APOA1):c.*19C>G	rs187335584	0.00029
NM_000039.3(APOA1):c.9T>C (p.Ala3=)	rs141383703	0.00006
NM_000039.3(APOA1):c.28G>A (p.Val10Met)	rs750125257	0.00003
NM_000039.3(APOA1):c.564C>G (p.Ala188=)	rs558064576

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