List of variants in gene CC2D2A reported as benign by PreventionGenetics, part of Exact Sciences

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.4065+28A>T	rs6832789	0.95451
NM_001378615.1(CC2D2A):c.247+26A>G	rs10000250	0.85216
NM_001378615.1(CC2D2A):c.1764+45T>G	rs1558572	0.75139
NM_001378615.1(CC2D2A):c.3183-8T>C	rs13121363	0.69106
NM_001378615.1(CC2D2A):c.3288+41A>C	rs13116304	0.68417
NM_001378615.1(CC2D2A):c.*21G>C	rs1134634	0.57021
NM_001378615.1(CC2D2A):c.1765-24A>G	rs1861044	0.52969
NM_001378615.1(CC2D2A):c.3595-22C>T	rs4280724	0.26375
NM_001378615.1(CC2D2A):c.3201G>A (p.Ser1067=)	rs73125627	0.20422
NM_001378615.1(CC2D2A):c.124-6C>T	rs1861049	0.15686
NM_001378615.1(CC2D2A):c.2182-24C>T	rs2041673	0.13698
NM_001378615.1(CC2D2A):c.2830-38G>T	rs35309200	0.12892
NM_001378615.1(CC2D2A):c.2003+19C>T	rs17476642	0.09677
NM_001378615.1(CC2D2A):c.156C>T (p.Ser52=)	rs1861050	0.07770
NM_001378615.1(CC2D2A):c.541-25G>T	rs16892080	0.04468
NM_001378615.1(CC2D2A):c.777C>T (p.His259=)	rs2286976	0.04284
NM_001378615.1(CC2D2A):c.1127A>C (p.Glu376Ala)	rs16892095	0.03933
NM_001378615.1(CC2D2A):c.721G>A (p.Glu241Lys)	rs62000428	0.00732
NM_001378615.1(CC2D2A):c.3509G>A (p.Arg1170Lys)	rs61734948	0.00656
NM_001378615.1(CC2D2A):c.1519A>G (p.Lys507Glu)	rs144439937	0.00644
NM_001378615.1(CC2D2A):c.2475C>T (p.Ile825=)	rs113835820	0.00275
NM_001378615.1(CC2D2A):c.4438-31T>C	rs147005127	0.00037
NM_001378615.1(CC2D2A):c.4438-9C>A	rs117667651	0.00036
NM_001378615.1(CC2D2A):c.501G>T (p.Lys167Asn)	rs190694237	0.00026
NM_001378615.1(CC2D2A):c.922T>C (p.Phe308Leu)	rs201465430	0.00009
NM_001378615.1(CC2D2A):c.1978G>C (p.Val660Leu)	rs16892134
NM_001378615.1(CC2D2A):c.676GAA[3] (p.Glu229del)	rs386833764

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