List of variants in gene CLDN16 reported as likely benign for calcinosis

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_006580.4(CLDN16):c.*181C>T	rs145675747	0.00570
NM_006580.4(CLDN16):c.626C>A (p.Ala209Asp)	rs139846352	0.00314
NM_006580.3(CLDN16):c.-41C>T	rs192579160	0.00298
NM_006580.4(CLDN16):c.*1952C>G	rs555889249	0.00266
NM_006580.4(CLDN16):c.165T>C (p.Phe55=)	rs144105475	0.00208
NM_006580.4(CLDN16):c.*1812A>G	rs138543261	0.00027
NM_006580.4(CLDN16):c.*1178C>T	rs533709248	0.00001
NM_006580.4(CLDN16):c.-45del	rs368234054

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