List of variants in gene CASR reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000388.4(CASR):c.73C>T (p.Arg25Ter)	rs201633414	0.00010
NM_000388.4(CASR):c.101T>C (p.Leu34Pro)	rs1559955362
NM_000388.4(CASR):c.1054T>G (p.Trp352Gly)
NM_000388.4(CASR):c.638C>T (p.Ala213Val)	rs1559958979

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