List of variants in gene CASR reported as pathogenic by Center for Bone Health, The Children's Hospital of Philadelphia

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.2429G>A (p.Ser810Asn)	rs2074938472
NM_000388.4(CASR):c.2465T>C (p.Ile822Thr)	rs1553769120
NM_000388.4(CASR):c.379G>A (p.Glu127Lys)	rs2074565202

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