ClinVar Miner

List of variants in gene DCC reported as uncertain significance for Mirror movements 1 and/or agenesis of the corpus callosum

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005215.4(DCC):c.3880G>A (p.Gly1294Arg)	rs532188333	0.00006
NM_005215.4(DCC):c.3620-2A>G	rs1292231805

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