List of variants in gene CC2D1A reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_017721.5(CC2D1A):c.980C>T (p.Ser327Leu)	rs200121704	0.00665
NM_017721.5(CC2D1A):c.1823+15C>G	rs139110235	0.00641
NM_017721.5(CC2D1A):c.1739C>T (p.Thr580Ile)	rs202057391	0.00476
NM_017721.5(CC2D1A):c.905G>A (p.Arg302Gln)	rs73922801	0.00283
NM_017721.5(CC2D1A):c.2440G>T (p.Ala814Ser)	rs56359259	0.00270
NM_017721.5(CC2D1A):c.1234A>G (p.Ile412Val)	rs191830054	0.00256

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