List of variants in gene APOA1 reported as benign for not provided

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000039.3(APOA1):c.200+33T>C	rs2070665	0.89533
NM_000039.3(APOA1):c.200+134T>C	rs5072	0.89522
NM_000039.3(APOA1):c.201-211T>C	rs7116797	0.76029
NM_000039.3(APOA1):c.43+41T>C	rs5070	0.60126
NC_000011.10:g.116835627T>C	rs12718463	0.15798
NM_000039.3(APOA1):c.201-63C>T	rs5076	0.11129
NM_000039.3(APOA1):c.-21+67C>T	rs5069	0.11111
NC_000011.10:g.116835630A>T	rs5081	0.06358
NM_000039.3(APOA1):c.201-274C>T	rs12718464	0.04460
NM_000039.3(APOA1):c.200+204G>A	rs5073	0.02025
NM_000039.3(APOA1):c.732C>G (p.Pro244=)	rs5080	0.00368
NM_000039.3(APOA1):c.181G>A (p.Ala61Thr)	rs12718465	0.00091

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