List of variants in gene MCCC2 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_022132.5(MCCC2):c.1368A>G (p.Ala456=)	rs10064079	0.82429
NM_022132.5(MCCC2):c.738+36G>A	rs12516456	0.80304
NM_022132.5(MCCC2):c.904-12A>G	rs277984	0.30658
NM_022132.5(MCCC2):c.999+39T>G	rs6891649	0.03059
NM_022132.5(MCCC2):c.739-25C>T	rs6861176	0.01639
NM_022132.5(MCCC2):c.1578A>G (p.Val526=)	rs114527907	0.01062
NM_022132.5(MCCC2):c.1439A>G (p.Asn480Ser)	rs115328026	0.00266

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