List of variants in gene CASR reported as likely benign by Sema4, Sema4

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000388.4(CASR):c.748G>A (p.Glu250Lys)	rs62269092	0.00163
NM_000388.4(CASR):c.6A>C (p.Ala2=)	rs112042188	0.00098
NM_000388.4(CASR):c.1631G>A (p.Arg544Gln)	rs115230894	0.00086
NM_000388.4(CASR):c.915C>A (p.Ile305=)	rs200528343	0.00051
NM_000388.4(CASR):c.2064C>T (p.Phe688=)	rs150869744	0.00037
NM_000388.4(CASR):c.1752G>A (p.Lys584=)	rs138638329	0.00014
NM_000388.4(CASR):c.201G>A (p.Gly67=)	rs1203051815	0.00001
NM_000388.4(CASR):c.738C>T (p.Tyr246=)	rs895337411	0.00001
NM_000388.4(CASR):c.3234A>G (p.Ser1078=)	rs556263764

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