List of variants in gene MCCC2 reported as benign by Illumina Laboratory Services, Illumina

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: 9

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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.*247C>T	rs1135667	0.78164
NM_022132.5(MCCC2):c.904-12A>G	rs277984	0.30658
NM_022132.5(MCCC2):c.*1198C>T	rs277975	0.28389
NM_022132.5(MCCC2):c.*593G>T	rs60069076	0.09309
NM_022132.5(MCCC2):c.*1573C>G	rs112693079	0.01960
NM_022132.5(MCCC2):c.*1381A>C	rs115650149	0.01118
NM_022132.5(MCCC2):c.1578A>G (p.Val526=)	rs114527907	0.01062
NM_022132.5(MCCC2):c.*1466T>C	rs148015309	0.00143

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