List of variants in gene KMT2A reported as uncertain significance for not specified

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001197104.2(KMT2A):c.1810A>G (p.Met604Val)	rs150328852	0.00046
NM_001197104.2(KMT2A):c.10835+1G>C	rs141515578	0.00004
NM_001197104.2(KMT2A):c.10901-5A>G	rs369909433	0.00002
NM_001197104.2(KMT2A):c.5287C>T (p.Arg1763Trp)	rs999060359	0.00001
NM_001197104.2(KMT2A):c.82G>T (p.Gly28Trp)	rs782113710	0.00001
NM_001197104.2(KMT2A):c.130C>A (p.Pro44Thr)	rs1437526128
NM_001197104.2(KMT2A):c.134C>G (p.Pro45Arg)	rs2134152876
NM_001197104.2(KMT2A):c.1877G>A (p.Arg626Lys)
NM_001197104.2(KMT2A):c.209G>A (p.Ser70Asn)	rs1177309170
NM_001197104.2(KMT2A):c.2905C>G (p.Leu969Val)	rs864309568
NM_001197104.2(KMT2A):c.3461G>A (p.Arg1154Gln)	rs1131691799
NM_001197104.2(KMT2A):c.6446G>C (p.Arg2149Pro)
NM_001197104.2(KMT2A):c.7193A>T (p.Glu2398Val)
NM_001197104.2(KMT2A):c.7463A>G (p.Asp2488Gly)
NM_001197104.2(KMT2A):c.841C>G (p.Leu281Val)
NM_001197104.2(KMT2A):c.8766A>C (p.Glu2922Asp)	rs2134400611
NM_001197104.2(KMT2A):c.9953G>C (p.Gly3318Ala)	rs1950572153

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