List of variants in gene KMT2B reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_014727.3(KMT2B):c.5276+8G>A	rs116914530	0.00798
NM_014727.3(KMT2B):c.1096G>A (p.Glu366Lys)	rs186777199	0.00442
NM_014727.3(KMT2B):c.2862C>T (p.Pro954=)	rs149968598	0.00416
NM_014727.3(KMT2B):c.5187C>T (p.Asn1729=)	rs34980546	0.00406
NM_014727.3(KMT2B):c.4489C>T (p.Leu1497=)	rs114437766	0.00388
NM_014727.3(KMT2B):c.2261C>T (p.Pro754Leu)	rs179686	0.00344
NM_014727.3(KMT2B):c.1760C>G (p.Pro587Arg)	rs2242519	0.00080
NM_014727.3(KMT2B):c.4219G>A (p.Gly1407Arg)	rs186268702	0.00048
NM_014727.3(KMT2B):c.4918-4G>A	rs201053288	0.00020

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