Variants in gene CDAN1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_138477.4(CDAN1):c.3450+11C>T	rs56046122	0.06311
NM_138477.4(CDAN1):c.2174+20G>A	rs75993383	0.02307
NM_138477.4(CDAN1):c.3194G>A (p.Arg1065Gln)	rs61746356	0.00932
NM_138477.4(CDAN1):c.1524A>G (p.Gln508=)	rs147500837	0.00283
NM_138477.4(CDAN1):c.2463G>A (p.Gly821=)	rs139809959	0.00204
NM_138477.4(CDAN1):c.2088G>A (p.Leu696=)	rs148759214	0.00023
NM_138477.4(CDAN1):c.639C>G (p.Thr213=)

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