List of variants in gene CASR reported as not provided for Bartter syndrome with hypocalcemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000388.4(CASR):c.2278A>T (p.Ile760Phe)	rs1453953571	0.00001
NM_000388.4(CASR):c.209G>A (p.Trp70Ter)	rs2107627458
NM_000388.4(CASR):c.494T>G (p.Val165Gly)	rs1559958757

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