U.S. flag

An official website of the United States government

Display Settings:

Format

Send to:

Choose Destination
1.

rs603893 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    C>T [Show Flanks]
    Chromosome:
    1:33633156 (GRCh38)
    1:34098756 (GRCh37)
    Canonical SPDI:
    NC_000001.11:33633155:C:T
    Gene:
    CSMD2 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    T=0.051492/6127 (ALFA)
    T=0.048096/48 (GoNL)
    T=0.060937/273 (Estonian)
    T=0.104027/31 (HapMap)
    T=0.107335/398 (TWINSUK)
    T=0.108459/418 (ALSPAC)
    T=0.12/72 (NorthernSweden)
    T=0.125/5 (GENOME_DK)
    T=0.139776/700 (1000Genomes)
    T=0.146285/21812 (GnomAD_genomes)
    T=0.15466/40937 (TOPMED)
    T=0.200968/1287 (1000Genomes_30X)
    T=0.214602/1552 (Korea4K)
    T=0.217747/638 (KOREAN)
    T=0.24537/53 (Qatari)
    T=0.323899/25084 (TOMMO)
    C=0.449275/62 (SGDP_PRJ)
    C=0.5/6 (Siberian)
    HGVS:

    Supplemental Content

    Search details

    See more...

    Recent activity