List of variants in gene KMT2B reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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_014727.3(KMT2B):c.4043A>G (p.Asn1348Ser)	rs1482613248	0.00001
NM_014727.3(KMT2B):c.5561C>T (p.Pro1854Leu)	rs374674556	0.00001
NM_014727.3(KMT2B):c.4792C>G (p.Leu1598Val)
NM_014727.3(KMT2B):c.6365G>A (p.Gly2122Glu)
NM_014727.3(KMT2B):c.6960-8C>T
NM_014727.3(KMT2B):c.7225C>T (p.Arg2409Trp)

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