List of variants reported as uncertain significance for Kleefstra syndrome 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_170606.3(KMT2C):c.6835C>A (p.Pro2279Thr)	rs775809939	0.00002
NM_170606.3(KMT2C):c.12194C>T (p.Ala4065Val)	rs141966811	0.00001
NM_170606.3(KMT2C):c.5851G>A (p.Asp1951Asn)	rs781220804	0.00001
NM_170606.3(KMT2C):c.709A>G (p.Ile237Val)	rs587778510	0.00001

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