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1.

rs35426722 has merged into rs3832043 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TT>-,T,TTT [Show Flanks]
    Chromosome:
    2:233671816 (GRCh38)
    2:234580462 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233671807:TTTTTTTTTT:TTTTTTTT,NC_000002.12:233671807:TTTTTTTTTT:TTTTTTTTT,NC_000002.12:233671807:TTTTTTTTTT:TTTTTTTTTTT
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TTTTTTTTTTT=0./0 (ALFA)
    T=0.29/174 (NorthernSweden)
    T=0.3/12 (GENOME_DK)
    T=0.327455/1467 (Estonian)
    T=0.346134/1334 (ALSPAC)
    T=0.377756/377 (GoNL)
    T=0.377832/1401 (TWINSUK)
    T=0.428403/113394 (TOPMED)
    T=0.448626/2243 (1000Genomes)
    HGVS:

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