ClinVar Miner

List of variants in gene CASR studied for Familial hypocalciuric hypercalcemia 1; Autosomal dominant hypocalcemia 1

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000388.4(CASR):c.2878C>T (p.Pro960Ser)	rs1352202616
NM_000388.4(CASR):c.294T>G (p.Phe98Leu)	rs878853976
NM_000388.4(CASR):c.508T>C (p.Ser170Pro)	rs1060502862

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