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1.

rs4253690 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>G [Show Flanks]
    Chromosome:
    22:46185026 (GRCh38)
    22:46580923 (GRCh37)
    Canonical SPDI:
    NC_000022.11:46185025:A:G
    Gene:
    PPARA (Varview)
    Functional Consequence:
    intron_variant,genic_upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.089057/4388 (ALFA)
    G=0.025/1 (GENOME_DK)
    G=0.045/27 (NorthernSweden)
    G=0.053191/10 (PharmGKB)
    G=0.060714/272 (Estonian)
    G=0.066132/66 (GoNL)
    G=0.075506/291 (ALSPAC)
    G=0.07767/288 (TWINSUK)
    G=0.0816/12158 (GnomAD_genomes)
    G=0.087963/19 (Qatari)
    G=0.088028/100 (Daghestan)
    G=0.089338/23647 (TOPMED)
    G=0.099781/639 (1000Genomes_30X)
    G=0.10004/501 (1000Genomes)
    G=0.115943/9124 (PAGE_STUDY)
    G=0.160377/34 (Vietnamese)
    G=0.193701/15001 (TOMMO)
    G=0.199392/1442 (Korea4K)
    G=0.206826/606 (KOREAN)
    A=0.428571/48 (SGDP_PRJ)
    A=0.4375/7 (Siberian)
    HGVS:

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