List of variants in gene SLC30A10 reported as likely benign for Hypermanganesemia with dystonia, polycythemia, and cirrhosis

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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_018713.3(SLC30A10):c.-87A>T	rs531545790	0.00315
NM_018713.3(SLC30A10):c.*945C>T	rs115277486	0.00246
NM_018713.3(SLC30A10):c.284C>T (p.Thr95Ile)	rs188273166	0.00060
NM_018713.3(SLC30A10):c.1272C>T (p.His424=)	rs544895572	0.00002
NM_018713.3(SLC30A10):c.*1188T>C	rs535541750	0.00001

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