List of variants in gene APOA1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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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.127G>A (p.Val43Met)	rs373545875	0.00002
NM_000039.3(APOA1):c.168G>A (p.Gln56=)	rs760886281	0.00002
NM_000039.3(APOA1):c.101G>T (p.Arg34Leu)	rs28929476	0.00001
NM_000039.3(APOA1):c.379G>A (p.Asp127Asn)	rs921646982	0.00001
NM_000039.3(APOA1):c.271G>T (p.Val91Leu)	rs2134231457

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