List of variants in gene SLC30A10 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_018713.3(SLC30A10):c.*744G>T	rs2275707	0.85119
NM_018713.3(SLC30A10):c.640+135T>G	rs79951865	0.56928
NM_018713.3(SLC30A10):c.959-62T>G	rs2231734	0.31485
NM_018713.3(SLC30A10):c.640+138T>G	rs76160931	0.28526
NM_018713.3(SLC30A10):c.640+141T>G	rs1383630862	0.12589
NM_018713.3(SLC30A10):c.640+120T>G	rs71521198	0.06246
NM_018713.3(SLC30A10):c.*276C>T	rs138571819	0.02157
NM_018713.3(SLC30A10):c.719-105A>C	rs6663795	0.01822
NM_018713.3(SLC30A10):c.640+16A>G	rs185021781	0.00489
NM_018713.3(SLC30A10):c.*1088G>A	rs2275706

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