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1.

rs35623965 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ->TA [Show Flanks]
    Chromosome:
    2:233715374 (GRCh38)
    2:234624021 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233715374:A:ATA
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A5 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    ATA=0.097246/1801 (ALFA)
    AT=0.069138/69 (GoNL)
    AT=0.085221/316 (TWINSUK)
    AT=0.089258/344 (ALSPAC)
    AT=0.096856/13574 (GnomAD)
    AT=0.102792/27208 (TOPMED)
    AT=0.121284/2033 (TOMMO)
    AT=0.125/5 (GENOME_DK)
    AT=0.13/78 (NorthernSweden)
    AT=0.140693/705 (1000Genomes)
    AT=0.155568/285 (Korea1K)
    HGVS:

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