List of variants in gene KMT2C reported as likely benign for Intellectual disability

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_170606.3(KMT2C):c.10513A>G (p.Asn3505Asp)	rs140626076	0.00036
NM_170606.3(KMT2C):c.2351C>A (p.Ser784Tyr)	rs780343727	0.00001
NM_170606.3(KMT2C):c.11008A>G (p.Asn3670Asp)	rs2092512174
NM_170606.3(KMT2C):c.2447dup (p.Tyr816Ter)	rs150073007
NM_170606.3(KMT2C):c.2698G>A (p.Gly900Arg)	rs1366232611
NM_170606.3(KMT2C):c.3194C>G (p.Ala1065Gly)	rs1284707010
NM_170606.3(KMT2C):c.6103C>A (p.Pro2035Thr)	rs1053658283
NM_170606.3(KMT2C):c.9801C>G (p.Ile3267Met)	rs2092584005

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