U.S. flag

An official website of the United States government

Display Settings:

Format

Send to:

Choose Destination
1.

rs4024061 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    2:233701489 (GRCh38)
    2:234610135 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233701488:C:T
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.018197/337 (ALFA)
    T=0.011667/7 (NorthernSweden)
    T=0.013889/3 (Qatari)
    T=0.015784/265 (TOMMO)
    T=0.026265/3680 (GnomAD)
    T=0.02778/7353 (TOPMED)
    T=0.031485/92 (KOREAN)
    T=0.03548/65 (Korea1K)
    T=0.040756/204 (1000Genomes)
    T=0.05/2 (GENOME_DK)
    C=0.482143/27 (SGDP_PRJ)
    HGVS:

    Supplemental Content

    Search details

    See more...

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...