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1.

rs5186 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    A>C [Show Flanks]
    Chromosome:
    3:148742201 (GRCh38)
    3:148459988 (GRCh37)
    Canonical SPDI:
    NC_000003.12:148742200:A:C
    Gene:
    AGTR1 (Varview)
    Functional Consequence:
    3_prime_UTR_variant
    Clinical significance:
    risk-factor,likely-benign,benign
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0.2745585/70019 (ALFA)
    C=0.0479798/38 (PRJEB37584)
    C=0.056815/411 (Korea4K)
    C=0.0600683/176 (KOREAN)
    C=0.0619902/38 (Vietnamese)
    C=0.0798512/6184 (TOMMO)
    C=0.1178115/590 (1000Genomes)
    C=0.1191443/763 (1000Genomes_30X)
    C=0.1296296/28 (Qatari)
    C=0.1414474/43 (FINRISK)
    C=0.1489035/11719 (PAGE_STUDY)
    C=0.1538462/8 (PRJEB36033)
    C=0.1702128/16 (PharmGKB)
    C=0.2041295/30450 (GnomAD_genomes)
    C=0.2068662/235 (Daghestan)
    C=0.2117118/56038 (TOPMED)
    C=0.2214859/1270 (GoESP)
    C=0.2229116/26444 (ExAC)
    C=0.2377232/1065 (Estonian)
    C=0.2533333/152 (NorthernSweden)
    C=0.2705264/359423 (GnomAD_exomes)
    C=0.2734082/146 (MGP)
    C=0.2988134/1108 (TWINSUK)
    C=0.3028023/1167 (ALSPAC)
    C=0.3186373/318 (GoNL)
    C=0.325/13 (GENOME_DK)
    A=0.375/6 (Siberian)
    A=0.4310345/50 (SGDP_PRJ)
    HGVS:

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