List of variants in gene CC2D2A reported as likely pathogenic by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.4667A>T (p.Asp1556Val)	rs201502401	0.00020
NM_001378615.1(CC2D2A):c.3976-3C>A	rs576298659
NM_001378615.1(CC2D2A):c.934G>A (p.Glu312Lys)	rs1716841949

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