List of variants in gene SLC12A6 reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001365088.1(SLC12A6):c.271+17825C>T	rs150751809	0.00276
NM_001365088.1(SLC12A6):c.1417A>G (p.Asn473Asp)	rs370477960	0.00019
NM_001365088.1(SLC12A6):c.221C>A (p.Ala74Glu)	rs373526599	0.00010
NM_001365088.1(SLC12A6):c.1601A>G (p.Asn534Ser)	rs778821191	0.00007
NM_001365088.1(SLC12A6):c.3427A>G (p.Ser1143Gly)	rs1322848611	0.00002
NM_001365088.1(SLC12A6):c.1118+4C>T	rs773294017	0.00001
NM_001365088.1(SLC12A6):c.1118+5G>A
NM_001365088.1(SLC12A6):c.1A>G (p.Met1Val)	rs1295560007
NM_001365088.1(SLC12A6):c.2110A>G (p.Ile704Val)	rs748542923
NM_001365088.1(SLC12A6):c.2T>C (p.Met1Thr)

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