ClinVar Miner

List of variants reported as uncertain significance for 3-methylcrotonyl-CoA carboxylase deficiency by Genomic Research Center, Shahid Beheshti University of Medical Sciences

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_020166.5(MCCC1):c.1701G>A (p.Thr567=)	rs377320336	0.00004
NM_020166.5(MCCC1):c.239G>A (p.Ser80Asn)	rs774565207	0.00001
NM_020166.5(MCCC1):c.794A>G (p.His265Arg)	rs759707763

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