List of variants in gene ABCC9 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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_020297.4(ABCC9):c.2770-13A>G	rs184123387	0.00055
NM_020297.4(ABCC9):c.2599G>A (p.Val867Ile)	rs376754153	0.00004
NM_020297.4(ABCC9):c.1616C>G (p.Ser539Cys)	rs1565470260
NM_020297.4(ABCC9):c.2848A>T (p.Met950Leu)	rs1448325219
NM_020297.4(ABCC9):c.4512+745dup	rs1555176123
NM_020297.4(ABCC9):c.614C>T (p.Pro205Leu)	rs1286474202

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