List of variants in gene combination KMT2C, LOC129999675 reported as likely benign

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_170606.3(KMT2C):c.11520A>T (p.Thr3840=)	rs747821479	0.00011
NM_170606.3(KMT2C):c.11570C>T (p.Thr3857Met)	rs577099359	0.00005
NM_170606.3(KMT2C):c.11534A>G (p.Glu3845Gly)	rs771124748	0.00003
NM_170606.3(KMT2C):c.11558G>A (p.Arg3853Gln)	rs751794784	0.00001
NM_170606.3(KMT2C):c.11515A>C (p.Lys3839Gln)
NM_170606.3(KMT2C):c.11549G>A (p.Arg3850Gln)	rs781280663

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