List of variants in gene SLC30A10 reported as pathogenic 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.1235del (p.Gln412fs)	rs281860292
NM_018713.3(SLC30A10):c.266T>C (p.Leu89Pro)	rs281860284
NM_018713.3(SLC30A10):c.314_322del (p.Ala105_Pro107del)	rs281860285
NM_018713.3(SLC30A10):c.507del (p.Pro170fs)	rs281860287
NM_018713.3(SLC30A10):c.585del (p.Thr196fs)	rs281860288

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