List of variants in gene KMT2C reported as uncertain significance for See cases

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_170606.3(KMT2C):c.11347A>G (p.Asn3783Asp)	rs2487684486
NM_170606.3(KMT2C):c.4918G>C (p.Glu1640Gln)	rs373510851
NM_170606.3(KMT2C):c.5416A>G (p.Ile1806Val)	rs1256350350
NM_170606.3(KMT2C):c.6841C>T (p.Pro2281Ser)	rs1488391618
NM_170606.3(KMT2C):c.9109_9111del (p.Leu3037del)	rs772433974
NM_170606.3(KMT2C):c.9397G>T (p.Val3133Leu)	rs984841454

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