List of variants in gene SLC4A4 reported as uncertain significance by GeneDx

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001098484.3(SLC4A4):c.1361C>T (p.Ala454Val)	rs138493429	0.00035
NM_001098484.3(SLC4A4):c.859G>A (p.Val287Met)	rs201871554	0.00002
NM_001098484.3(SLC4A4):c.2774G>A (p.Arg925His)	rs1736599400

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