Variants in gene SLC12A3 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001126108.2(SLC12A3):c.2711G>A (p.Arg904Gln)	rs11643718	0.08543
NM_001126108.2(SLC12A3):c.1925+72C>G	rs12596776	0.08327
NM_001126108.2(SLC12A3):c.1865A>G (p.Asn622Ser)	rs61746763	0.01359
NM_001126108.2(SLC12A3):c.2182G>A (p.Ala728Thr)	rs36049418	0.01075
NM_001126108.2(SLC12A3):c.2857-6G>A	rs117981500	0.00557
NM_001126108.2(SLC12A3):c.1539C>T (p.Tyr513=)	rs146805986	0.00544
NM_001126108.2(SLC12A3):c.774C>T (p.Asn258=)	rs111578437	0.00523
NM_001126108.2(SLC12A3):c.2083G>A (p.Gly695Arg)	rs36031476	0.00473
NM_001126108.2(SLC12A3):c.249G>T (p.Arg83=)	rs76750525	0.00420
NM_001126108.2(SLC12A3):c.307C>T (p.Leu103=)	rs35005216	0.00257
NM_001126108.2(SLC12A3):c.1210G>A (p.Val404Ile)	rs150358489	0.00196
NM_001126108.2(SLC12A3):c.1392C>A (p.Ala464=)	rs118121751	0.00146
NM_001126108.2(SLC12A3):c.93C>T (p.Pro31=)	rs34055681	0.00143
NM_001126108.2(SLC12A3):c.2190C>T (p.Leu730=)	rs150692587	0.00141
NM_001126108.2(SLC12A3):c.363G>C (p.Glu121Asp)	rs146632606	0.00101
NM_001126108.2(SLC12A3):c.429+9G>A	rs375425173	0.00091
NM_001126108.2(SLC12A3):c.2286-18C>T	rs201972617	0.00084
NM_001126108.2(SLC12A3):c.2285+8G>A	rs199854613	0.00061
NM_001126108.2(SLC12A3):c.36C>T (p.Asp12=)	rs117987946	0.00061
NM_001126108.2(SLC12A3):c.1386C>T (p.Phe462=)	rs142199602	0.00048
NM_001126108.2(SLC12A3):c.1543A>G (p.Ile515Val)	rs554432544	0.00033
NM_001126108.2(SLC12A3):c.2368+8C>A	rs140236327	0.00015
NM_001126108.2(SLC12A3):c.1176C>T (p.Thr392=)	rs117440321
NM_001126108.2(SLC12A3):c.791= (p.Ala264=)

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