Variants in gene CASR with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 5

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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.1189G>A (p.Gly397Arg)	rs1064794291	0.00001
NM_000388.4(CASR):c.2915C>T (p.Thr972Met)	rs200620134	0.00001
NM_000388.4(CASR):c.1913G>T (p.Arg638Leu)	rs201852643
NM_000388.4(CASR):c.2770_2777del (p.Phe924fs)	rs2473281810

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