ClinVar Miner

List of variants in gene CASR reported as uncertain significance by Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000388.4(CASR):c.848T>C (p.Ile283Thr)	rs142745096	0.00007
NM_000388.4(CASR):c.610T>A (p.Phe204Ile)	rs1060499700

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