Display Settings:

Format

Send to:

Choose Destination
1.

rs13398413 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>G [Show Flanks]
    Chromosome:
    2:77753565 (GRCh38)
    2:77980691 (GRCh37)
    Canonical SPDI:
    NC_000002.12:77753564:C:G
    Gene:
    LOC101927967 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.081366/1537 (ALFA)
    G=0.027148/455 (TOMMO)
    G=0.032205/59 (Korea1K)
    G=0.044148/129 (KOREAN)
    G=0.057143/256 (Estonian)
    G=0.068241/263 (ALSPAC)
    G=0.069444/15 (Qatari)
    G=0.069444/15 (Vietnamese)
    G=0.075/3 (GENOME_DK)
    G=0.075/45 (NorthernSweden)
    G=0.076591/284 (TWINSUK)
    G=0.088858/445 (1000Genomes)
    G=0.089178/89 (GoNL)
    G=0.093856/13109 (GnomAD)
    G=0.094813/25096 (TOPMED)
    G=0.121951/40 (HapMap)
    C=0.459459/34 (SGDP_PRJ)
    C=0.5/3 (Siberian)
    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...
    Support Center