Variants in gene SLC12A3 with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.1145C>T (p.Thr382Met)	rs187885782	0.00006
NM_001126108.2(SLC12A3):c.2863C>T (p.Arg955Trp)	rs559626481	0.00006
NM_001126108.2(SLC12A3):c.434G>A (p.Arg145His)	rs374324018	0.00005
NM_001126108.2(SLC12A3):c.2546T>A (p.Leu849His)	rs185927948	0.00001
NM_001126108.2(SLC12A3):c.403C>T (p.Arg135Cys)	rs749742102	0.00001
NM_001126108.2(SLC12A3):c.587G>T (p.Gly196Val)	rs1290372649	0.00001
NM_001126108.2(SLC12A3):c.184G>A (p.Asp62Asn)	rs757490496
NM_001126108.2(SLC12A3):c.209A>G (p.Tyr70Cys)

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