List of variants reported as uncertain significance for calcium metabolic disease by Institute of Human Genetics, Cologne University

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000388.4(CASR):c.1693T>C (p.Cys565Arg)	rs1559967708
NM_000388.4(CASR):c.2339C>A (p.Thr780Asn)	rs754332943
NM_000388.4(CASR):c.2637C>G (p.His879Gln)	rs1576878230
NM_000388.4(CASR):c.516A>T (p.Arg172Ser)	rs1114167368
NM_002067.5(GNA11):c.95A>G (p.Asp32Gly)	rs200234790

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