Variants in gene CASR with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
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.2064C>T (p.Phe688=)	rs150869744	0.00037
NM_000388.4(CASR):c.1110G>A (p.Val370=)	rs150412204	0.00027
NM_000388.4(CASR):c.2777A>G (p.Gln926Arg)	rs200263975	0.00012
NM_000388.4(CASR):c.1188A>G (p.Thr396=)	rs200312817	0.00008
NM_000388.4(CASR):c.779A>G (p.Gln260Arg)	rs200386687	0.00005
NM_000388.4(CASR):c.60C>T (p.Tyr20=)	rs201564143	0.00004
NM_000388.4(CASR):c.1668G>A (p.Glu556=)	rs186279271	0.00003
NM_000388.4(CASR):c.1297G>C (p.Asp433His)	rs199511990	0.00001
NM_000388.4(CASR):c.2901C>A (p.Ile967=)	rs199594582

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