U.S. flag

An official website of the United States government

Display Settings:

Format

Send to:

Choose Destination
1.

rs45437594 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>C [Show Flanks]
    Chromosome:
    2:233683200 (GRCh38)
    2:234591846 (GRCh37)
    Canonical SPDI:
    NC_000002.12:233683199:T:C
    Gene:
    UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A9 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.000794/15 (ALFA)
    C=0.00087/122 (GnomAD)
    C=0.001186/314 (TOPMED)
    C=0.001563/7 (Estonian)
    C=0.005309/27 (1000Genomes)
    C=0.006944/1 (PharmGKB)
    C=0.028037/6 (Vietnamese)
    C=0.036275/608 (TOMMO)
    C=0.039014/114 (KOREAN)
    T=0.5/2 (SGDP_PRJ)
    HGVS:

    Supplemental Content

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...