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1.

rs369735173 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A [Show Flanks]
    Chromosome:
    19:2213896
    Gene:
    DOT1L (Varview)
    Functional Consequence:
    synonymous_variant,coding_sequence_variant
    Validated:
    by frequency,by cluster
    MAF:
    A=0.000024/3 (TOPMED)
    A=0.000032/1 (GnomAD)
    A=0.002359/586 (GnomAD_exomes)
    A=0.002715/323 (ExAC)
    A=0.005791/29 (1000Genomes)
    HGVS:
    NC_000019.10:g.2213896G>A, NC_000019.9:g.2213895G>A, NG_029793.1:g.54748G>A, NM_032482.3:c.1707G>A, NM_032482.2:c.1707G>A, XM_005259659.3:c.1707G>A, XM_005259659.1:c.1707G>A, XM_005259660.3:c.1707G>A, XM_005259660.1:c.1707G>A, XM_011528359.2:c.1707G>A, XM_011528361.2:c.837G>A, XM_017027366.1:c.1050G>A, XM_011528360.1:c.1497G>A

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