List of variants in gene MCCC1 reported as benign by Pars Genome Lab

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_020166.5(MCCC1):c.1978-57G>T	rs6786878	0.93354
NM_020166.5(MCCC1):c.396C>T (p.Leu132=)	rs7622479	0.89165
NM_020166.5(MCCC1):c.1391A>C (p.His464Pro)	rs2270968	0.58081
NM_020166.5(MCCC1):c.369+96C>T	rs6806083	0.54587
NM_020166.5(MCCC1):c.1594+39T>C	rs2270969	0.06776
NM_020166.5(MCCC1):c.1681+77C>T	rs75187429	0.06739
NM_020166.5(MCCC1):c.1732-208T>C	rs2108441955
NM_020166.5(MCCC1):c.1978-86A>C	rs2292056
NM_020166.5(MCCC1):c.273+53A>C	rs3732604

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