Variants in gene SLC4A1 with conflicting interpretations "likely benign" and "pathogenic"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_000342.3(SLC4A1):c.118G>A (p.Glu40Lys)	rs45562031	0.01150
NM_000342.4(SLC4A1):c.2561C>T (p.Pro854Leu)	rs2285644	0.00284
NM_000342.4(SLC4A1):c.2603C>T (p.Pro868Leu)	rs121912759	0.00051
NM_000342.4(SLC4A1):c.1937G>A (p.Arg646Gln)	rs121912757	0.00004

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