List of variants in gene CC2D2A reported as likely benign by Eurofins NTD LLC (GA)

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001378615.1(CC2D2A):c.2475C>T (p.Ile825=)	rs113835820	0.00275
NM_001378615.1(CC2D2A):c.4459C>T (p.Arg1487Cys)	rs186486235	0.00265
NM_001378615.1(CC2D2A):c.2804G>A (p.Arg935Gln)	rs187003641	0.00142
NM_001378615.1(CC2D2A):c.2813T>C (p.Met938Thr)	rs61740537	0.00123
NM_001378615.1(CC2D2A):c.351T>G (p.Ser117Arg)	rs186264635	0.00120
NM_001378615.1(CC2D2A):c.1162G>A (p.Val388Ile)	rs115924432	0.00089
NM_001378615.1(CC2D2A):c.3872T>C (p.Ile1291Thr)	rs370492044	0.00009
NM_001378615.1(CC2D2A):c.922T>C (p.Phe308Leu)	rs201465430	0.00009
NM_001378615.1(CC2D2A):c.4238G>A (p.Cys1413Tyr)	rs146843542	0.00007
NM_001378615.1(CC2D2A):c.1978G>C (p.Val660Leu)	rs16892134
NM_001378615.1(CC2D2A):c.2922+10dup	rs752271495

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