List of variants in gene SLC8A3 reported as likely benign

Minimum submission review status:		Collection method:
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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_182932.3(SLC8A3):c.572A>G (p.Asp191Gly)	rs79418648	0.00247
NM_182932.3(SLC8A3):c.2172C>T (p.Tyr724=)	rs149109491	0.00006
NM_182932.3(SLC8A3):c.1889-3699C>T	rs774149200	0.00001
NM_182932.3(SLC8A3):c.2730C>T (p.Ala910=)	rs1363074115	0.00001
NM_182932.3(SLC8A3):c.1404A>C (p.Ile468=)	rs1308562252

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