List of variants in gene combination KMT2C, LOC123956272 reported as uncertain significance for Kleefstra syndrome 2

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Gene type: Distinguish antisense genes from sense genes
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_170606.3(KMT2C):c.1042G>A (p.Asp348Asn)	rs201834857	0.00013
NM_170606.3(KMT2C):c.1013-2A>G	rs751158858
NM_170606.3(KMT2C):c.1106T>C (p.Met369Thr)

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