{{Rsnum
|rsid=231591
|Gene=KMT2B
|Chromosome=19
|position=35733804
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|GMAF=0.4362
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=KMT2B
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 26.6 | 53.1 | 20.3
| HCB | 31.1 | 46.7 | 22.2
| JPT | 31.8 | 47.7 | 20.5
| YRI | 66.1 | 32.3 | 1.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 31.1 | 46.7 | 22.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

{{Venter SNP
|rsid=231591
|allele=G
|frequency=0.466
|uid=1103691136789
|type=heterozygous_SNP
|hugo=MLL4_HUMAN
|ensembl gene=ENSG00000105663
|ensembl transcript=ENST00000222270
|sift=
|disease=Often amplified in pancreatic carcinomas.
}}

{{GET Evidence
|gene=NM_014727
|aa_change=Asp2361Gly
|aa_change_short=D2361G
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs231591
|overall_frequency_n=5686
|overall_frequency_d=9864
|overall_frequency=0.57644
|n_genomes=49
|n_genomes_annotated=0
|n_haplomes=78
|n_articles=0
|n_articles_annotated=0
|nblosum100=4
|autoscore=0
|webscore=N
}}

{{on chip | HumanOmni1Quad}}