List of variants in gene MCCC2 reported as likely 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_022132.5(MCCC2):c.*1351G>A	rs144494459	0.01269
NM_022132.5(MCCC2):c.*245T>C	rs11551918	0.01133
NM_022132.5(MCCC2):c.*1080G>T	rs7727902	0.01132
NM_022132.5(MCCC2):c.*577T>A	rs150412501	0.00871
NM_022132.5(MCCC2):c.1569C>T (p.Ser523=)	rs137961577	0.00003
NM_022132.5(MCCC2):c.*970G>A	rs368250327

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