ClinVar Miner

List of variants in gene ABCC9 reported as uncertain significance by Genetics and Genomics Program, Sidra Medicine

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_020297.4(ABCC9):c.2950C>T (p.Arg984Cys)	rs78979794	0.00001
NM_020297.4(ABCC9):c.588C>G (p.Phe196Leu)	rs1948583041

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