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1.

rs1611430 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>A,C,T [Show Flanks]
    Chromosome:
    6:29925684 (GRCh38)
    6:29893461 (GRCh37)
    Canonical SPDI:
    NC_000006.12:29925683:G:A,NC_000006.12:29925683:G:C,NC_000006.12:29925683:G:T
    Gene:
    HCG4B (Varview)
    Functional Consequence:
    non_coding_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    G=0.149664/2491 (ALFA)
    G=0.008629/582 (TOMMO)
    G=0.015789/3 (Vietnamese)
    G=0.020766/142 (Korea4K)
    G=0.027937/78 (KOREAN)
    G=0.036145/18 (SGDP_PRJ)
    G=0.05/2 (GENOME_DK)
    G=0.087859/440 (1000Genomes)
    G=0.087914/563 (1000Genomes_30X)
    G=0.107477/23 (Qatari)
    G=0.13977/19963 (GnomAD_genomes)
    G=0.166667/8 (Siberian)
    G=0.181818/108 (NorthernSweden)
    G=0.232465/232 (GoNL)
    G=0.397004/212 (MGP)
    G=0.45977/80 (Korea1K)
    HGVS:
    NC_000006.12:g.29925684G>A, NC_000006.12:g.29925684G>C, NC_000006.12:g.29925684G>T, NC_000006.11:g.29893461G>A, NC_000006.11:g.29893461G>C, NC_000006.11:g.29893461G>T, NT_113891.3:g.1407078A>G, NT_113891.3:g.1407078A>C, NT_113891.3:g.1407078A>T, NT_113891.2:g.1407184A>G, NT_113891.2:g.1407184A>C, NT_113891.2:g.1407184A>T, NT_167248.2:g.1182512A>G, NT_167248.2:g.1182512A>C, NT_167248.2:g.1182512A>T, NT_167248.1:g.1188108A>G, NT_167248.1:g.1188108A>C, NT_167248.1:g.1188108A>T, NT_167245.2:g.1182882A>G, NT_167245.2:g.1182882A>C, NT_167245.2:g.1182882A>T, NT_167245.1:g.1188467A>G, NT_167245.1:g.1188467A>C, NT_167245.1:g.1188467A>T, NT_167249.2:g.1225419A>G, NT_167249.2:g.1225419A>C, NT_167249.2:g.1225419A>T, NT_167249.1:g.1224717A>G, NT_167249.1:g.1224717A>C, NT_167249.1:g.1224717A>T, NT_167246.2:g.1182091A>G, NT_167246.2:g.1182091A>C, NT_167246.2:g.1182091A>T, NT_167246.1:g.1187711A>G, NT_167246.1:g.1187711A>C, NT_167246.1:g.1187711A>T, NT_167244.2:g.1185404A>G, NT_167244.2:g.1185404A>C, NT_167244.2:g.1185404A>T, NW_003871063.1:g.161581A>G, NW_003871063.1:g.161581A>C, NW_003871063.1:g.161581A>T, NT_167244.1:g.1135320A>G, NT_167244.1:g.1135320A>C, NT_167244.1:g.1135320A>T, NR_001317.3:n.1532C>T, NR_001317.3:n.1532C>G, NR_001317.3:n.1532C>A, NR_001317.2:n.1489T>C, NR_001317.2:n.1489T>G, NR_001317.2:n.1489T>A

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