List of variants in gene CASR reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000388.4(CASR):c.1333A>G (p.Thr445Ala)	rs12493789	0.01436
NM_000388.4(CASR):c.1631G>A (p.Arg544Gln)	rs115230894	0.00086
NM_000388.4(CASR):c.3091G>A (p.Gly1031Ser)	rs142704083	0.00061
NM_000388.4(CASR):c.1192G>A (p.Asp398Asn)	rs201177696	0.00052
NM_000388.4(CASR):c.779A>G (p.Gln260Arg)	rs200386687	0.00005
NM_000388.4(CASR):c.2295C>T (p.Cys765=)	rs1232096655	0.00001
NM_000388.4(CASR):c.1686C>T (p.Cys562=)	rs193922428
NM_000388.4(CASR):c.3063G>A (p.Thr1021=)	rs193922440
NM_000388.4(CASR):c.3153C>T (p.Ser1051=)	rs1576879292
NM_000388.4(CASR):c.876C>T (p.Ile292=)	rs772232871

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