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1.

rs34874998 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    A>- [Show Flanks]
    Chromosome:
    4:69484442 (GRCh38)
    4:70350160 (GRCh37)
    Canonical SPDI:
    NC_000004.12:69484441:AAAAA:AAAA
    Gene:
    UGT2B4 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    AAAA=0./0 (ALFA)
    -=0.000007/1 (GnomAD)
    HGVS:

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