List of variants in gene SLC12A2 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001046.3(SLC12A2):c.788A>C (p.Glu263Ala)	rs367694835	0.00011
NM_001046.3(SLC12A2):c.2210T>A (p.Leu737Gln)	rs376802988	0.00001
NM_001046.3(SLC12A2):c.2293C>G (p.Leu765Val)	rs548545596	0.00001
NM_001046.3(SLC12A2):c.1127A>G (p.Asn376Ser)	rs116621105
NM_001046.3(SLC12A2):c.2848G>A (p.Val950Met)	rs760024899
NM_001046.3(SLC12A2):c.3622C>G (p.Leu1208Val)	rs761150347
NM_001046.3(SLC12A2):c.881G>A (p.Arg294His)	rs1484832467

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