Variants in gene CC2D2A with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.4340A>C (p.Glu1447Ala)	rs387907058	0.00004
NM_001378615.1(CC2D2A):c.100C>T (p.Arg34Ter)	rs896947430	0.00002
NM_001378615.1(CC2D2A):c.3596T>C (p.Ile1199Thr)	rs760918829	0.00002
NM_001378615.1(CC2D2A):c.2999A>T (p.Glu1000Val)	rs773881370	0.00001
NM_001378615.1(CC2D2A):c.3364C>T (p.Pro1122Ser)	rs118204051
NM_001378615.1(CC2D2A):c.4533G>C (p.Trp1511Cys)	rs777158229

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