Variants in gene CDHR1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_033100.4(CDHR1):c.240C>T (p.Val80=)	rs11593005	0.00943
NM_033100.4(CDHR1):c.2041-15G>A	rs61867367	0.00830
NM_033100.4(CDHR1):c.1868A>G (p.Asn623Ser)	rs137876961	0.00404
NM_033100.4(CDHR1):c.1071C>T (p.Ser357=)	rs146588811	0.00167
NM_033100.4(CDHR1):c.526-7C>G	rs190906755	0.00166
NM_033100.4(CDHR1):c.1461G>A (p.Gly487=)	rs141787212	0.00145
NM_033100.4(CDHR1):c.2229G>A (p.Arg743=)	rs150969538	0.00106
NM_033100.4(CDHR1):c.159C>A (p.His53Gln)	rs12781048
NM_033100.4(CDHR1):c.2473C>A (p.Pro825Thr)	rs201515900

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