ClinVar Miner

List of variants in gene KMT2C reported as benign for Kleefstra syndrome 2

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_170606.3(KMT2C):c.8685G>A (p.Gln2895=)	rs6464211	0.33944
NM_170606.3(KMT2C):c.2769+5G>T	rs73728782	0.00022

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