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

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_138477.2(CDAN1):c.2015C>T (p.Pro672Leu)	rs120074167	0.00013
NM_138477.4(CDAN1):c.156C>G (p.Phe52Leu)	rs80338694	0.00009
NM_138477.4(CDAN1):c.2140C>T (p.Arg714Trp)	rs80338696	0.00008
NM_138477.4(CDAN1):c.3389C>T (p.Pro1130Leu)	rs80338699	0.00005

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