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Items: 1 to 20 of 840

1.

rs1491333661 [Homo sapiens]
    Variant type:
    INS
    Alleles:
    ->A [Show Flanks]
    Chromosome:
    11:27657780 (GRCh38)
    11:27679328 (GRCh37)
    Canonical SPDI:
    NC_000011.10:27657780::A
    Gene:
    BDNF (Varview), BDNF-AS (Varview)
    Functional Consequence:
    3_prime_UTR_variant,intron_variant
    HGVS:
    NC_000011.10:g.27657780_27657781insA, NC_000011.9:g.27679327_27679328insA, NG_011794.1:g.69278_69279insT, NM_170735.6:c.*40_*41insT, NM_170735.5:c.*40_*41insT, NM_170731.5:c.*40_*41insT, NM_170731.4:c.*40_*41insT, NM_001709.5:c.*40_*41insT, NM_001709.4:c.*40_*41insT, NM_170732.4:c.*40_*41insT, NM_170733.4:c.*40_*41insT, NM_170733.3:c.*40_*41insT, NM_170734.4:c.*40_*41insT, NM_170734.3:c.*40_*41insT, NM_001143816.2:c.*40_*41insT, NM_001143816.1:c.*40_*41insT, NM_001143811.2:c.*40_*41insT, NM_001143811.1:c.*40_*41insT, NM_001143814.2:c.*40_*41insT, NM_001143814.1:c.*40_*41insT, NM_001143810.2:c.*40_*41insT, NM_001143810.1:c.*40_*41insT, NM_001143813.2:c.*40_*41insT, NM_001143813.1:c.*40_*41insT, NM_001143812.2:c.*40_*41insT, NM_001143812.1:c.*40_*41insT, NM_001143809.2:c.*40_*41insT, NM_001143809.1:c.*40_*41insT, NM_001143808.2:c.*40_*41insT, NM_001143808.1:c.*40_*41insT, NM_001143807.2:c.*40_*41insT, NM_001143807.1:c.*40_*41insT, NM_001143806.1:c.*40_*41insT, NM_001143805.1:c.*40_*41insT, NM_001143815.1:c.*40_*41insT

    2.

    rs1490825385 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      T>C [Show Flanks]
      Chromosome:
      11:27656795 (GRCh38)
      11:27678342 (GRCh37)
      Canonical SPDI:
      NC_000011.10:27656794:T:C
      Gene:
      BDNF (Varview), BDNF-AS (Varview)
      Functional Consequence:
      3_prime_UTR_variant,intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      C=0./0 (ALFA)
      C=0.000007/1 (GnomAD)
      HGVS:
      NC_000011.10:g.27656795T>C, NC_000011.9:g.27678342T>C, NG_011794.1:g.70263A>G, NM_170735.6:c.*1026A>G, NM_170735.5:c.*1025A>G, NM_170731.5:c.*1026A>G, NM_170731.4:c.*1025A>G, NM_001709.5:c.*1026A>G, NM_001709.4:c.*1025A>G, NM_170732.4:c.*1025A>G, NM_170733.4:c.*1026A>G, NM_170733.3:c.*1025A>G, NM_170734.4:c.*1026A>G, NM_170734.3:c.*1025A>G, NM_001143816.2:c.*1026A>G, NM_001143816.1:c.*1025A>G, NM_001143811.2:c.*1026A>G, NM_001143811.1:c.*1025A>G, NM_001143814.2:c.*1026A>G, NM_001143814.1:c.*1025A>G, NM_001143810.2:c.*1026A>G, NM_001143810.1:c.*1025A>G, NM_001143813.2:c.*1026A>G, NM_001143813.1:c.*1025A>G, NM_001143812.2:c.*1026A>G, NM_001143812.1:c.*1025A>G, NM_001143809.2:c.*1026A>G, NM_001143809.1:c.*1025A>G, NM_001143808.2:c.*1026A>G, NM_001143808.1:c.*1025A>G, NM_001143807.2:c.*1026A>G, NM_001143807.1:c.*1025A>G, NM_001143806.1:c.*1025A>G, NM_001143805.1:c.*1025A>G, NM_001143815.1:c.*1025A>G

      3.

      rs1489423068 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        A>G [Show Flanks]
        Chromosome:
        11:27656510 (GRCh38)
        11:27678057 (GRCh37)
        Canonical SPDI:
        NC_000011.10:27656509:A:G
        Gene:
        BDNF (Varview), BDNF-AS (Varview)
        Functional Consequence:
        3_prime_UTR_variant,intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        G=0./0 (ALFA)
        G=0.000007/1 (GnomAD)
        HGVS:
        NC_000011.10:g.27656510A>G, NC_000011.9:g.27678057A>G, NG_011794.1:g.70548T>C, NM_170735.6:c.*1311T>C, NM_170735.5:c.*1310T>C, NM_170731.5:c.*1311T>C, NM_170731.4:c.*1310T>C, NM_001709.5:c.*1311T>C, NM_001709.4:c.*1310T>C, NM_170732.4:c.*1310T>C, NM_170733.4:c.*1311T>C, NM_170733.3:c.*1310T>C, NM_170734.4:c.*1311T>C, NM_170734.3:c.*1310T>C, NM_001143816.2:c.*1311T>C, NM_001143816.1:c.*1310T>C, NM_001143811.2:c.*1311T>C, NM_001143811.1:c.*1310T>C, NM_001143814.2:c.*1311T>C, NM_001143814.1:c.*1310T>C, NM_001143810.2:c.*1311T>C, NM_001143810.1:c.*1310T>C, NM_001143813.2:c.*1311T>C, NM_001143813.1:c.*1310T>C, NM_001143812.2:c.*1311T>C, NM_001143812.1:c.*1310T>C, NM_001143809.2:c.*1311T>C, NM_001143809.1:c.*1310T>C, NM_001143808.2:c.*1311T>C, NM_001143808.1:c.*1310T>C, NM_001143807.2:c.*1311T>C, NM_001143807.1:c.*1310T>C, NM_001143806.1:c.*1310T>C, NM_001143805.1:c.*1310T>C, NM_001143815.1:c.*1310T>C

        4.

        rs1488864054 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          C>T [Show Flanks]
          Chromosome:
          11:27658401 (GRCh38)
          11:27679948 (GRCh37)
          Canonical SPDI:
          NC_000011.10:27658400:C:T
          Gene:
          BDNF (Varview), BDNF-AS (Varview)
          Functional Consequence:
          non_coding_transcript_variant,missense_variant,coding_sequence_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          T=0./0 (ALFA)
          T=0.000004/1 (TOPMED)
          HGVS:
          NC_000011.10:g.27658401C>T, NC_000011.9:g.27679948C>T, NG_011794.1:g.68658G>A, NM_170735.6:c.164G>A, NM_170735.5:c.164G>A, NM_170731.5:c.188G>A, NM_170731.4:c.188G>A, NM_001709.5:c.164G>A, NM_001709.4:c.164G>A, NM_170732.4:c.164G>A, NM_170733.4:c.164G>A, NM_170733.3:c.164G>A, NM_170734.4:c.209G>A, NM_170734.3:c.209G>A, NM_001143816.2:c.164G>A, NM_001143816.1:c.164G>A, NM_001143811.2:c.164G>A, NM_001143811.1:c.164G>A, NM_001143814.2:c.164G>A, NM_001143814.1:c.164G>A, NM_001143810.2:c.410G>A, NM_001143810.1:c.410G>A, NM_001143813.2:c.164G>A, NM_001143813.1:c.164G>A, NM_001143812.2:c.164G>A, NM_001143812.1:c.164G>A, NM_001143809.2:c.251G>A, NM_001143809.1:c.251G>A, NM_001143808.2:c.164G>A, NM_001143808.1:c.164G>A, NM_001143807.2:c.164G>A, NM_001143807.1:c.164G>A, NM_001143806.1:c.164G>A, NM_001143805.1:c.164G>A, NR_002832.2:n.535C>T, NR_033312.1:n.466C>T, NR_033314.1:n.535C>T, NR_033315.1:n.466C>T, NR_033313.1:n.466C>T, NM_001143815.1:c.164G>A, NP_733931.1:p.Gly55Asp, NP_733927.1:p.Gly63Asp, NP_001700.2:p.Gly55Asp, NP_733928.1:p.Gly55Asp, NP_733929.1:p.Gly55Asp, NP_733930.1:p.Gly70Asp, NP_001137288.1:p.Gly55Asp, NP_001137283.1:p.Gly55Asp, NP_001137286.1:p.Gly55Asp, NP_001137282.1:p.Gly137Asp, NP_001137285.1:p.Gly55Asp, NP_001137284.1:p.Gly55Asp, NP_001137281.1:p.Gly84Asp, NP_001137280.1:p.Gly55Asp, NP_001137279.1:p.Gly55Asp, NP_001137278.1:p.Gly55Asp, NP_001137277.1:p.Gly55Asp

          5.

          rs1488566227 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            T>G [Show Flanks]
            Chromosome:
            11:27656827 (GRCh38)
            11:27678374 (GRCh37)
            Canonical SPDI:
            NC_000011.10:27656826:T:G
            Gene:
            BDNF (Varview), BDNF-AS (Varview)
            Functional Consequence:
            3_prime_UTR_variant,intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            G=0./0 (ALFA)
            G=0.000004/1 (TOPMED)
            G=0.000007/1 (GnomAD)
            HGVS:
            NC_000011.10:g.27656827T>G, NC_000011.9:g.27678374T>G, NG_011794.1:g.70231A>C, NM_170735.6:c.*994A>C, NM_170735.5:c.*993A>C, NM_170731.5:c.*994A>C, NM_170731.4:c.*993A>C, NM_001709.5:c.*994A>C, NM_001709.4:c.*993A>C, NM_170732.4:c.*993A>C, NM_170733.4:c.*994A>C, NM_170733.3:c.*993A>C, NM_170734.4:c.*994A>C, NM_170734.3:c.*993A>C, NM_001143816.2:c.*994A>C, NM_001143816.1:c.*993A>C, NM_001143811.2:c.*994A>C, NM_001143811.1:c.*993A>C, NM_001143814.2:c.*994A>C, NM_001143814.1:c.*993A>C, NM_001143810.2:c.*994A>C, NM_001143810.1:c.*993A>C, NM_001143813.2:c.*994A>C, NM_001143813.1:c.*993A>C, NM_001143812.2:c.*994A>C, NM_001143812.1:c.*993A>C, NM_001143809.2:c.*994A>C, NM_001143809.1:c.*993A>C, NM_001143808.2:c.*994A>C, NM_001143808.1:c.*993A>C, NM_001143807.2:c.*994A>C, NM_001143807.1:c.*993A>C, NM_001143806.1:c.*993A>C, NM_001143805.1:c.*993A>C, NM_001143815.1:c.*993A>C

            6.

            rs1488545532 has merged into rs1262566140 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              C>-,CC,CCC [Show Flanks]
              Chromosome:
              11:27657279 (GRCh38)
              11:27678826 (GRCh37)
              Canonical SPDI:
              NC_000011.10:27657278:CCCCCC:CCCCC,NC_000011.10:27657278:CCCCCC:CCCCCCC,NC_000011.10:27657278:CCCCCC:CCCCCCCC
              Gene:
              BDNF (Varview), BDNF-AS (Varview)
              Functional Consequence:
              3_prime_UTR_variant,intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              CCCCCCCC=0./0 (ALFA)
              -=0.00016/1 (1000Genomes)
              -=0.00022/1 (Estonian)
              HGVS:
              NC_000011.10:g.27657284del, NC_000011.10:g.27657284dup, NC_000011.10:g.27657283_27657284dup, NC_000011.9:g.27678831del, NC_000011.9:g.27678831dup, NC_000011.9:g.27678830_27678831dup, NG_011794.1:g.69779del, NG_011794.1:g.69779dup, NG_011794.1:g.69778_69779dup, NM_170735.6:c.*542del, NM_170735.6:c.*542dup, NM_170735.6:c.*541_*542dup, NM_170735.5:c.*541del, NM_170735.5:c.*541dup, NM_170735.5:c.*540_*541dup, NM_170731.5:c.*542del, NM_170731.5:c.*542dup, NM_170731.5:c.*541_*542dup, NM_170731.4:c.*541del, NM_170731.4:c.*541dup, NM_170731.4:c.*540_*541dup, NM_001709.5:c.*542del, NM_001709.5:c.*542dup, NM_001709.5:c.*541_*542dup, NM_001709.4:c.*541del, NM_001709.4:c.*541dup, NM_001709.4:c.*540_*541dup, NM_170732.4:c.*541del, NM_170732.4:c.*541dup, NM_170732.4:c.*540_*541dup, NM_170733.4:c.*542del, NM_170733.4:c.*542dup, NM_170733.4:c.*541_*542dup, NM_170733.3:c.*541del, NM_170733.3:c.*541dup, NM_170733.3:c.*540_*541dup, NM_170734.4:c.*542del, NM_170734.4:c.*542dup, NM_170734.4:c.*541_*542dup, NM_170734.3:c.*541del, NM_170734.3:c.*541dup, NM_170734.3:c.*540_*541dup, NM_001143816.2:c.*542del, NM_001143816.2:c.*542dup, NM_001143816.2:c.*541_*542dup, NM_001143816.1:c.*541del, NM_001143816.1:c.*541dup, NM_001143816.1:c.*540_*541dup, NM_001143811.2:c.*542del, NM_001143811.2:c.*542dup, NM_001143811.2:c.*541_*542dup, NM_001143811.1:c.*541del, NM_001143811.1:c.*541dup, NM_001143811.1:c.*540_*541dup, NM_001143814.2:c.*542del, NM_001143814.2:c.*542dup, NM_001143814.2:c.*541_*542dup, NM_001143814.1:c.*541del, NM_001143814.1:c.*541dup, NM_001143814.1:c.*540_*541dup, NM_001143810.2:c.*542del, NM_001143810.2:c.*542dup, NM_001143810.2:c.*541_*542dup, NM_001143810.1:c.*541del, NM_001143810.1:c.*541dup, NM_001143810.1:c.*540_*541dup, NM_001143813.2:c.*542del, NM_001143813.2:c.*542dup, NM_001143813.2:c.*541_*542dup, NM_001143813.1:c.*541del, NM_001143813.1:c.*541dup, NM_001143813.1:c.*540_*541dup, NM_001143812.2:c.*542del, NM_001143812.2:c.*542dup, NM_001143812.2:c.*541_*542dup, NM_001143812.1:c.*541del, NM_001143812.1:c.*541dup, NM_001143812.1:c.*540_*541dup, NM_001143809.2:c.*542del, NM_001143809.2:c.*542dup, NM_001143809.2:c.*541_*542dup, NM_001143809.1:c.*541del, NM_001143809.1:c.*541dup, NM_001143809.1:c.*540_*541dup, NM_001143808.2:c.*542del, NM_001143808.2:c.*542dup, NM_001143808.2:c.*541_*542dup, NM_001143808.1:c.*541del, NM_001143808.1:c.*541dup, NM_001143808.1:c.*540_*541dup, NM_001143807.2:c.*542del, NM_001143807.2:c.*542dup, NM_001143807.2:c.*541_*542dup, NM_001143807.1:c.*541del, NM_001143807.1:c.*541dup, NM_001143807.1:c.*540_*541dup, NM_001143806.1:c.*541del, NM_001143806.1:c.*541dup, NM_001143806.1:c.*540_*541dup, NM_001143805.1:c.*541del, NM_001143805.1:c.*541dup, NM_001143805.1:c.*540_*541dup, NM_001143815.1:c.*541del, NM_001143815.1:c.*541dup, NM_001143815.1:c.*540_*541dup

              7.

              rs1487785831 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>A [Show Flanks]
                Chromosome:
                11:27656923 (GRCh38)
                11:27678470 (GRCh37)
                Canonical SPDI:
                NC_000011.10:27656922:C:A
                Gene:
                BDNF (Varview), BDNF-AS (Varview)
                Functional Consequence:
                3_prime_UTR_variant,intron_variant
                Validated:
                by frequency,by alfa
                MAF:
                A=0./0 (ALFA)
                A=0.000008/2 (TOPMED)
                HGVS:
                NC_000011.10:g.27656923C>A, NC_000011.9:g.27678470C>A, NG_011794.1:g.70135G>T, NM_170735.6:c.*898G>T, NM_170735.5:c.*897G>T, NM_170731.5:c.*898G>T, NM_170731.4:c.*897G>T, NM_001709.5:c.*898G>T, NM_001709.4:c.*897G>T, NM_170732.4:c.*897G>T, NM_170733.4:c.*898G>T, NM_170733.3:c.*897G>T, NM_170734.4:c.*898G>T, NM_170734.3:c.*897G>T, NM_001143816.2:c.*898G>T, NM_001143816.1:c.*897G>T, NM_001143811.2:c.*898G>T, NM_001143811.1:c.*897G>T, NM_001143814.2:c.*898G>T, NM_001143814.1:c.*897G>T, NM_001143810.2:c.*898G>T, NM_001143810.1:c.*897G>T, NM_001143813.2:c.*898G>T, NM_001143813.1:c.*897G>T, NM_001143812.2:c.*898G>T, NM_001143812.1:c.*897G>T, NM_001143809.2:c.*898G>T, NM_001143809.1:c.*897G>T, NM_001143808.2:c.*898G>T, NM_001143808.1:c.*897G>T, NM_001143807.2:c.*898G>T, NM_001143807.1:c.*897G>T, NM_001143806.1:c.*897G>T, NM_001143805.1:c.*897G>T, NM_001143815.1:c.*897G>T

                8.

                rs1487457372 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  C>G [Show Flanks]
                  Chromosome:
                  11:27657269 (GRCh38)
                  11:27678816 (GRCh37)
                  Canonical SPDI:
                  NC_000011.10:27657268:C:G
                  Gene:
                  BDNF (Varview), BDNF-AS (Varview)
                  Functional Consequence:
                  3_prime_UTR_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0./0 (ALFA)
                  G=0.000004/1 (TOPMED)
                  G=0.000007/1 (GnomAD)
                  HGVS:
                  NC_000011.10:g.27657269C>G, NC_000011.9:g.27678816C>G, NG_011794.1:g.69789G>C, NM_170735.6:c.*552G>C, NM_170735.5:c.*551G>C, NM_170731.5:c.*552G>C, NM_170731.4:c.*551G>C, NM_001709.5:c.*552G>C, NM_001709.4:c.*551G>C, NM_170732.4:c.*551G>C, NM_170733.4:c.*552G>C, NM_170733.3:c.*551G>C, NM_170734.4:c.*552G>C, NM_170734.3:c.*551G>C, NM_001143816.2:c.*552G>C, NM_001143816.1:c.*551G>C, NM_001143811.2:c.*552G>C, NM_001143811.1:c.*551G>C, NM_001143814.2:c.*552G>C, NM_001143814.1:c.*551G>C, NM_001143810.2:c.*552G>C, NM_001143810.1:c.*551G>C, NM_001143813.2:c.*552G>C, NM_001143813.1:c.*551G>C, NM_001143812.2:c.*552G>C, NM_001143812.1:c.*551G>C, NM_001143809.2:c.*552G>C, NM_001143809.1:c.*551G>C, NM_001143808.2:c.*552G>C, NM_001143808.1:c.*551G>C, NM_001143807.2:c.*552G>C, NM_001143807.1:c.*551G>C, NM_001143806.1:c.*551G>C, NM_001143805.1:c.*551G>C, NM_001143815.1:c.*551G>C

                  9.

                  rs1485333590 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    A>T [Show Flanks]
                    Chromosome:
                    11:27655946 (GRCh38)
                    11:27677493 (GRCh37)
                    Canonical SPDI:
                    NC_000011.10:27655945:A:T
                    Gene:
                    BDNF (Varview), BDNF-AS (Varview)
                    Functional Consequence:
                    3_prime_UTR_variant,intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    T=0./0 (ALFA)
                    T=0.000004/1 (TOPMED)
                    HGVS:
                    NC_000011.10:g.27655946A>T, NC_000011.9:g.27677493A>T, NG_011794.1:g.71112T>A, NM_170735.6:c.*1875T>A, NM_170735.5:c.*1874T>A, NM_170731.5:c.*1875T>A, NM_170731.4:c.*1874T>A, NM_001709.5:c.*1875T>A, NM_001709.4:c.*1874T>A, NM_170732.4:c.*1874T>A, NM_170733.4:c.*1875T>A, NM_170733.3:c.*1874T>A, NM_170734.4:c.*1875T>A, NM_170734.3:c.*1874T>A, NM_001143816.2:c.*1875T>A, NM_001143816.1:c.*1874T>A, NM_001143811.2:c.*1875T>A, NM_001143811.1:c.*1874T>A, NM_001143814.2:c.*1875T>A, NM_001143814.1:c.*1874T>A, NM_001143810.2:c.*1875T>A, NM_001143810.1:c.*1874T>A, NM_001143813.2:c.*1875T>A, NM_001143813.1:c.*1874T>A, NM_001143812.2:c.*1875T>A, NM_001143812.1:c.*1874T>A, NM_001143809.2:c.*1875T>A, NM_001143809.1:c.*1874T>A, NM_001143808.2:c.*1875T>A, NM_001143808.1:c.*1874T>A, NM_001143807.2:c.*1875T>A, NM_001143807.1:c.*1874T>A, NM_001143806.1:c.*1874T>A, NM_001143805.1:c.*1874T>A, NM_001143815.1:c.*1874T>A

                    10.

                    rs1484561925 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>C,T [Show Flanks]
                      Chromosome:
                      11:27656991 (GRCh38)
                      11:27678538 (GRCh37)
                      Canonical SPDI:
                      NC_000011.10:27656990:G:C,NC_000011.10:27656990:G:T
                      Gene:
                      BDNF (Varview), BDNF-AS (Varview)
                      Functional Consequence:
                      3_prime_UTR_variant,intron_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      T=0./0 (ALFA)
                      T=0.000004/1 (TOPMED)
                      HGVS:
                      NC_000011.10:g.27656991G>C, NC_000011.10:g.27656991G>T, NC_000011.9:g.27678538G>C, NC_000011.9:g.27678538G>T, NG_011794.1:g.70067C>G, NG_011794.1:g.70067C>A, NM_170735.6:c.*830C>G, NM_170735.6:c.*830C>A, NM_170735.5:c.*829C>G, NM_170735.5:c.*829C>A, NM_170731.5:c.*830C>G, NM_170731.5:c.*830C>A, NM_170731.4:c.*829C>G, NM_170731.4:c.*829C>A, NM_001709.5:c.*830C>G, NM_001709.5:c.*830C>A, NM_001709.4:c.*829C>G, NM_001709.4:c.*829C>A, NM_170732.4:c.*829C>G, NM_170732.4:c.*829C>A, NM_170733.4:c.*830C>G, NM_170733.4:c.*830C>A, NM_170733.3:c.*829C>G, NM_170733.3:c.*829C>A, NM_170734.4:c.*830C>G, NM_170734.4:c.*830C>A, NM_170734.3:c.*829C>G, NM_170734.3:c.*829C>A, NM_001143816.2:c.*830C>G, NM_001143816.2:c.*830C>A, NM_001143816.1:c.*829C>G, NM_001143816.1:c.*829C>A, NM_001143811.2:c.*830C>G, NM_001143811.2:c.*830C>A, NM_001143811.1:c.*829C>G, NM_001143811.1:c.*829C>A, NM_001143814.2:c.*830C>G, NM_001143814.2:c.*830C>A, NM_001143814.1:c.*829C>G, NM_001143814.1:c.*829C>A, NM_001143810.2:c.*830C>G, NM_001143810.2:c.*830C>A, NM_001143810.1:c.*829C>G, NM_001143810.1:c.*829C>A, NM_001143813.2:c.*830C>G, NM_001143813.2:c.*830C>A, NM_001143813.1:c.*829C>G, NM_001143813.1:c.*829C>A, NM_001143812.2:c.*830C>G, NM_001143812.2:c.*830C>A, NM_001143812.1:c.*829C>G, NM_001143812.1:c.*829C>A, NM_001143809.2:c.*830C>G, NM_001143809.2:c.*830C>A, NM_001143809.1:c.*829C>G, NM_001143809.1:c.*829C>A, NM_001143808.2:c.*830C>G, NM_001143808.2:c.*830C>A, NM_001143808.1:c.*829C>G, NM_001143808.1:c.*829C>A, NM_001143807.2:c.*830C>G, NM_001143807.2:c.*830C>A, NM_001143807.1:c.*829C>G, NM_001143807.1:c.*829C>A, NM_001143806.1:c.*829C>G, NM_001143806.1:c.*829C>A, NM_001143805.1:c.*829C>G, NM_001143805.1:c.*829C>A, NM_001143815.1:c.*829C>G, NM_001143815.1:c.*829C>A

                      11.

                      rs1484516038 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>A [Show Flanks]
                        Chromosome:
                        11:27656047 (GRCh38)
                        11:27677594 (GRCh37)
                        Canonical SPDI:
                        NC_000011.10:27656046:G:A
                        Gene:
                        BDNF (Varview), BDNF-AS (Varview)
                        Functional Consequence:
                        3_prime_UTR_variant,intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        A=0./0 (ALFA)
                        A=0.000007/1 (GnomAD)
                        A=0.000008/2 (TOPMED)
                        HGVS:
                        NC_000011.10:g.27656047G>A, NC_000011.9:g.27677594G>A, NG_011794.1:g.71011C>T, NM_170735.6:c.*1774C>T, NM_170735.5:c.*1773C>T, NM_170731.5:c.*1774C>T, NM_170731.4:c.*1773C>T, NM_001709.5:c.*1774C>T, NM_001709.4:c.*1773C>T, NM_170732.4:c.*1773C>T, NM_170733.4:c.*1774C>T, NM_170733.3:c.*1773C>T, NM_170734.4:c.*1774C>T, NM_170734.3:c.*1773C>T, NM_001143816.2:c.*1774C>T, NM_001143816.1:c.*1773C>T, NM_001143811.2:c.*1774C>T, NM_001143811.1:c.*1773C>T, NM_001143814.2:c.*1774C>T, NM_001143814.1:c.*1773C>T, NM_001143810.2:c.*1774C>T, NM_001143810.1:c.*1773C>T, NM_001143813.2:c.*1774C>T, NM_001143813.1:c.*1773C>T, NM_001143812.2:c.*1774C>T, NM_001143812.1:c.*1773C>T, NM_001143809.2:c.*1774C>T, NM_001143809.1:c.*1773C>T, NM_001143808.2:c.*1774C>T, NM_001143808.1:c.*1773C>T, NM_001143807.2:c.*1774C>T, NM_001143807.1:c.*1773C>T, NM_001143806.1:c.*1773C>T, NM_001143805.1:c.*1773C>T, NM_001143815.1:c.*1773C>T

                        12.

                        rs1484057256 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          C>T [Show Flanks]
                          Chromosome:
                          11:27658151 (GRCh38)
                          11:27679698 (GRCh37)
                          Canonical SPDI:
                          NC_000011.10:27658150:C:T
                          Gene:
                          BDNF (Varview), BDNF-AS (Varview)
                          Functional Consequence:
                          intron_variant,coding_sequence_variant,synonymous_variant
                          Validated:
                          by frequency
                          MAF:
                          T=0.000004/1 (GnomAD_exomes)
                          HGVS:
                          NC_000011.10:g.27658151C>T, NC_000011.9:g.27679698C>T, NG_011794.1:g.68908G>A, NM_170735.6:c.414G>A, NM_170735.5:c.414G>A, NM_170731.5:c.438G>A, NM_170731.4:c.438G>A, NM_001709.5:c.414G>A, NM_001709.4:c.414G>A, NM_170732.4:c.414G>A, NM_170733.4:c.414G>A, NM_170733.3:c.414G>A, NM_170734.4:c.459G>A, NM_170734.3:c.459G>A, NM_001143816.2:c.414G>A, NM_001143816.1:c.414G>A, NM_001143811.2:c.414G>A, NM_001143811.1:c.414G>A, NM_001143814.2:c.414G>A, NM_001143814.1:c.414G>A, NM_001143810.2:c.660G>A, NM_001143810.1:c.660G>A, NM_001143813.2:c.414G>A, NM_001143813.1:c.414G>A, NM_001143812.2:c.414G>A, NM_001143812.1:c.414G>A, NM_001143809.2:c.501G>A, NM_001143809.1:c.501G>A, NM_001143808.2:c.414G>A, NM_001143808.1:c.414G>A, NM_001143807.2:c.414G>A, NM_001143807.1:c.414G>A, NM_001143806.1:c.414G>A, NM_001143805.1:c.414G>A, NM_001143815.1:c.414G>A

                          13.

                          rs1482939898 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>T [Show Flanks]
                            Chromosome:
                            11:27658487 (GRCh38)
                            11:27680034 (GRCh37)
                            Canonical SPDI:
                            NC_000011.10:27658486:G:T
                            Gene:
                            BDNF (Varview), BDNF-AS (Varview)
                            Functional Consequence:
                            intron_variant,coding_sequence_variant,synonymous_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            T=0.000004/1 (TOPMED)
                            T=0.000014/2 (GnomAD)
                            HGVS:
                            NC_000011.10:g.27658487G>T, NC_000011.9:g.27680034G>T, NG_011794.1:g.68572C>A, NM_170735.6:c.78C>A, NM_170735.5:c.78C>A, NM_170731.5:c.102C>A, NM_170731.4:c.102C>A, NM_001709.5:c.78C>A, NM_001709.4:c.78C>A, NM_170732.4:c.78C>A, NM_170733.4:c.78C>A, NM_170733.3:c.78C>A, NM_170734.4:c.123C>A, NM_170734.3:c.123C>A, NM_001143816.2:c.78C>A, NM_001143816.1:c.78C>A, NM_001143811.2:c.78C>A, NM_001143811.1:c.78C>A, NM_001143814.2:c.78C>A, NM_001143814.1:c.78C>A, NM_001143810.2:c.324C>A, NM_001143810.1:c.324C>A, NM_001143813.2:c.78C>A, NM_001143813.1:c.78C>A, NM_001143812.2:c.78C>A, NM_001143812.1:c.78C>A, NM_001143809.2:c.165C>A, NM_001143809.1:c.165C>A, NM_001143808.2:c.78C>A, NM_001143808.1:c.78C>A, NM_001143807.2:c.78C>A, NM_001143807.1:c.78C>A, NM_001143806.1:c.78C>A, NM_001143805.1:c.78C>A, NM_001143815.1:c.78C>A

                            14.

                            rs1481378865 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>C [Show Flanks]
                              Chromosome:
                              11:27657512 (GRCh38)
                              11:27679059 (GRCh37)
                              Canonical SPDI:
                              NC_000011.10:27657511:T:C
                              Gene:
                              BDNF (Varview), BDNF-AS (Varview)
                              Functional Consequence:
                              intron_variant,3_prime_UTR_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0./0 (ALFA)
                              C=0.000004/1 (TOPMED)
                              C=0.000007/1 (GnomAD)
                              HGVS:
                              NC_000011.10:g.27657512T>C, NC_000011.9:g.27679059T>C, NG_011794.1:g.69547A>G, NM_170735.6:c.*309A>G, NM_170735.5:c.*309A>G, NM_170731.5:c.*309A>G, NM_170731.4:c.*309A>G, NM_001709.5:c.*309A>G, NM_001709.4:c.*309A>G, NM_170732.4:c.*309A>G, NM_170733.4:c.*309A>G, NM_170733.3:c.*309A>G, NM_170734.4:c.*309A>G, NM_170734.3:c.*309A>G, NM_001143816.2:c.*309A>G, NM_001143816.1:c.*309A>G, NM_001143811.2:c.*309A>G, NM_001143811.1:c.*309A>G, NM_001143814.2:c.*309A>G, NM_001143814.1:c.*309A>G, NM_001143810.2:c.*309A>G, NM_001143810.1:c.*309A>G, NM_001143813.2:c.*309A>G, NM_001143813.1:c.*309A>G, NM_001143812.2:c.*309A>G, NM_001143812.1:c.*309A>G, NM_001143809.2:c.*309A>G, NM_001143809.1:c.*309A>G, NM_001143808.2:c.*309A>G, NM_001143808.1:c.*309A>G, NM_001143807.2:c.*309A>G, NM_001143807.1:c.*309A>G, NM_001143806.1:c.*309A>G, NM_001143805.1:c.*309A>G, NM_001143815.1:c.*309A>G

                              15.

                              rs1480522575 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>A [Show Flanks]
                                Chromosome:
                                11:27657690 (GRCh38)
                                11:27679237 (GRCh37)
                                Canonical SPDI:
                                NC_000011.10:27657689:G:A
                                Gene:
                                BDNF (Varview), BDNF-AS (Varview)
                                Functional Consequence:
                                intron_variant,3_prime_UTR_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                A=0.000071/1 (ALFA)
                                A=0.000004/1 (TOPMED)
                                HGVS:
                                NC_000011.10:g.27657690G>A, NC_000011.9:g.27679237G>A, NG_011794.1:g.69369C>T, NM_170735.6:c.*131C>T, NM_170735.5:c.*131C>T, NM_170731.5:c.*131C>T, NM_170731.4:c.*131C>T, NM_001709.5:c.*131C>T, NM_001709.4:c.*131C>T, NM_170732.4:c.*131C>T, NM_170733.4:c.*131C>T, NM_170733.3:c.*131C>T, NM_170734.4:c.*131C>T, NM_170734.3:c.*131C>T, NM_001143816.2:c.*131C>T, NM_001143816.1:c.*131C>T, NM_001143811.2:c.*131C>T, NM_001143811.1:c.*131C>T, NM_001143814.2:c.*131C>T, NM_001143814.1:c.*131C>T, NM_001143810.2:c.*131C>T, NM_001143810.1:c.*131C>T, NM_001143813.2:c.*131C>T, NM_001143813.1:c.*131C>T, NM_001143812.2:c.*131C>T, NM_001143812.1:c.*131C>T, NM_001143809.2:c.*131C>T, NM_001143809.1:c.*131C>T, NM_001143808.2:c.*131C>T, NM_001143808.1:c.*131C>T, NM_001143807.2:c.*131C>T, NM_001143807.1:c.*131C>T, NM_001143806.1:c.*131C>T, NM_001143805.1:c.*131C>T, NM_001143815.1:c.*131C>T

                                16.

                                rs1480353411 [Homo sapiens]
                                  Variant type:
                                  DEL
                                  Alleles:
                                  G>- [Show Flanks]
                                  Chromosome:
                                  11:27655601 (GRCh38)
                                  11:27677148 (GRCh37)
                                  Canonical SPDI:
                                  NC_000011.10:27655600:G:
                                  Gene:
                                  BDNF (Varview), BDNF-AS (Varview)
                                  Functional Consequence:
                                  intron_variant,3_prime_UTR_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  -=0./0 (ALFA)
                                  HGVS:
                                  NC_000011.10:g.27655601del, NC_000011.9:g.27677148del, NG_011794.1:g.71457del, NM_170735.6:c.*2220del, NM_170735.5:c.*2219del, NM_170731.5:c.*2220del, NM_170731.4:c.*2219del, NM_001709.5:c.*2220del, NM_001709.4:c.*2219del, NM_170732.4:c.*2219del, NM_170733.4:c.*2220del, NM_170733.3:c.*2219del, NM_170734.4:c.*2220del, NM_170734.3:c.*2219del, NM_001143816.2:c.*2220del, NM_001143816.1:c.*2219del, NM_001143811.2:c.*2220del, NM_001143811.1:c.*2219del, NM_001143814.2:c.*2220del, NM_001143814.1:c.*2219del, NM_001143810.2:c.*2220del, NM_001143810.1:c.*2219del, NM_001143813.2:c.*2220del, NM_001143813.1:c.*2219del, NM_001143812.2:c.*2220del, NM_001143812.1:c.*2219del, NM_001143809.2:c.*2220del, NM_001143809.1:c.*2219del, NM_001143808.2:c.*2220del, NM_001143808.1:c.*2219del, NM_001143807.2:c.*2220del, NM_001143807.1:c.*2219del, NM_001143806.1:c.*2219del, NM_001143805.1:c.*2219del, NM_001143815.1:c.*2219del

                                  17.

                                  rs1477458422 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>C [Show Flanks]
                                    Chromosome:
                                    11:27657817 (GRCh38)
                                    11:27679364 (GRCh37)
                                    Canonical SPDI:
                                    NC_000011.10:27657816:T:C
                                    Gene:
                                    BDNF (Varview), BDNF-AS (Varview)
                                    Functional Consequence:
                                    intron_variant,3_prime_UTR_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    C=0.000028/1 (ALFA)
                                    C=0.000007/1 (GnomAD)
                                    C=0.000008/2 (GnomAD_exomes)
                                    C=0.000011/3 (TOPMED)
                                    HGVS:
                                    NC_000011.10:g.27657817T>C, NC_000011.9:g.27679364T>C, NG_011794.1:g.69242A>G, NM_170735.6:c.*4A>G, NM_170735.5:c.*4A>G, NM_170731.5:c.*4A>G, NM_170731.4:c.*4A>G, NM_001709.5:c.*4A>G, NM_001709.4:c.*4A>G, NM_170732.4:c.*4A>G, NM_170733.4:c.*4A>G, NM_170733.3:c.*4A>G, NM_170734.4:c.*4A>G, NM_170734.3:c.*4A>G, NM_001143816.2:c.*4A>G, NM_001143816.1:c.*4A>G, NM_001143811.2:c.*4A>G, NM_001143811.1:c.*4A>G, NM_001143814.2:c.*4A>G, NM_001143814.1:c.*4A>G, NM_001143810.2:c.*4A>G, NM_001143810.1:c.*4A>G, NM_001143813.2:c.*4A>G, NM_001143813.1:c.*4A>G, NM_001143812.2:c.*4A>G, NM_001143812.1:c.*4A>G, NM_001143809.2:c.*4A>G, NM_001143809.1:c.*4A>G, NM_001143808.2:c.*4A>G, NM_001143808.1:c.*4A>G, NM_001143807.2:c.*4A>G, NM_001143807.1:c.*4A>G, NM_001143806.1:c.*4A>G, NM_001143805.1:c.*4A>G, NM_001143815.1:c.*4A>G

                                    18.

                                    rs1476927388 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>G [Show Flanks]
                                      Chromosome:
                                      11:27657302 (GRCh38)
                                      11:27678849 (GRCh37)
                                      Canonical SPDI:
                                      NC_000011.10:27657301:C:G
                                      Gene:
                                      BDNF (Varview), BDNF-AS (Varview)
                                      Functional Consequence:
                                      intron_variant,3_prime_UTR_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      G=0./0 (ALFA)
                                      G=0.000004/1 (TOPMED)
                                      HGVS:
                                      NC_000011.10:g.27657302C>G, NC_000011.9:g.27678849C>G, NG_011794.1:g.69756G>C, NM_170735.6:c.*519G>C, NM_170735.5:c.*518G>C, NM_170731.5:c.*519G>C, NM_170731.4:c.*518G>C, NM_001709.5:c.*519G>C, NM_001709.4:c.*518G>C, NM_170732.4:c.*518G>C, NM_170733.4:c.*519G>C, NM_170733.3:c.*518G>C, NM_170734.4:c.*519G>C, NM_170734.3:c.*518G>C, NM_001143816.2:c.*519G>C, NM_001143816.1:c.*518G>C, NM_001143811.2:c.*519G>C, NM_001143811.1:c.*518G>C, NM_001143814.2:c.*519G>C, NM_001143814.1:c.*518G>C, NM_001143810.2:c.*519G>C, NM_001143810.1:c.*518G>C, NM_001143813.2:c.*519G>C, NM_001143813.1:c.*518G>C, NM_001143812.2:c.*519G>C, NM_001143812.1:c.*518G>C, NM_001143809.2:c.*519G>C, NM_001143809.1:c.*518G>C, NM_001143808.2:c.*519G>C, NM_001143808.1:c.*518G>C, NM_001143807.2:c.*519G>C, NM_001143807.1:c.*518G>C, NM_001143806.1:c.*518G>C, NM_001143805.1:c.*518G>C, NM_001143815.1:c.*518G>C

                                      19.

                                      rs1476899405 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>T [Show Flanks]
                                        Chromosome:
                                        11:27658404 (GRCh38)
                                        11:27679951 (GRCh37)
                                        Canonical SPDI:
                                        NC_000011.10:27658403:C:T
                                        Gene:
                                        BDNF (Varview), BDNF-AS (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,missense_variant,non_coding_transcript_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        T=0./0 (ALFA)
                                        T=0.000004/1 (TOPMED)
                                        HGVS:
                                        NC_000011.10:g.27658404C>T, NC_000011.9:g.27679951C>T, NG_011794.1:g.68655G>A, NM_170735.6:c.161G>A, NM_170735.5:c.161G>A, NM_170731.5:c.185G>A, NM_170731.4:c.185G>A, NM_001709.5:c.161G>A, NM_001709.4:c.161G>A, NM_170732.4:c.161G>A, NM_170733.4:c.161G>A, NM_170733.3:c.161G>A, NM_170734.4:c.206G>A, NM_170734.3:c.206G>A, NM_001143816.2:c.161G>A, NM_001143816.1:c.161G>A, NM_001143811.2:c.161G>A, NM_001143811.1:c.161G>A, NM_001143814.2:c.161G>A, NM_001143814.1:c.161G>A, NM_001143810.2:c.407G>A, NM_001143810.1:c.407G>A, NM_001143813.2:c.161G>A, NM_001143813.1:c.161G>A, NM_001143812.2:c.161G>A, NM_001143812.1:c.161G>A, NM_001143809.2:c.248G>A, NM_001143809.1:c.248G>A, NM_001143808.2:c.161G>A, NM_001143808.1:c.161G>A, NM_001143807.2:c.161G>A, NM_001143807.1:c.161G>A, NM_001143806.1:c.161G>A, NM_001143805.1:c.161G>A, NR_002832.2:n.538C>T, NR_033312.1:n.469C>T, NR_033314.1:n.538C>T, NR_033315.1:n.469C>T, NR_033313.1:n.469C>T, NM_001143815.1:c.161G>A, NP_733931.1:p.Arg54Lys, NP_733927.1:p.Arg62Lys, NP_001700.2:p.Arg54Lys, NP_733928.1:p.Arg54Lys, NP_733929.1:p.Arg54Lys, NP_733930.1:p.Arg69Lys, NP_001137288.1:p.Arg54Lys, NP_001137283.1:p.Arg54Lys, NP_001137286.1:p.Arg54Lys, NP_001137282.1:p.Arg136Lys, NP_001137285.1:p.Arg54Lys, NP_001137284.1:p.Arg54Lys, NP_001137281.1:p.Arg83Lys, NP_001137280.1:p.Arg54Lys, NP_001137279.1:p.Arg54Lys, NP_001137278.1:p.Arg54Lys, NP_001137277.1:p.Arg54Lys

                                        20.

                                        rs1475656593 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>C [Show Flanks]
                                          Chromosome:
                                          11:27655585 (GRCh38)
                                          11:27677132 (GRCh37)
                                          Canonical SPDI:
                                          NC_000011.10:27655584:T:C
                                          Gene:
                                          BDNF (Varview), BDNF-AS (Varview)
                                          Functional Consequence:
                                          intron_variant,3_prime_UTR_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          C=0./0 (ALFA)
                                          C=0.000011/3 (TOPMED)
                                          HGVS:
                                          NC_000011.10:g.27655585T>C, NC_000011.9:g.27677132T>C, NG_011794.1:g.71473A>G, NM_170735.6:c.*2236A>G, NM_170735.5:c.*2235A>G, NM_170731.5:c.*2236A>G, NM_170731.4:c.*2235A>G, NM_001709.5:c.*2236A>G, NM_001709.4:c.*2235A>G, NM_170732.4:c.*2235A>G, NM_170733.4:c.*2236A>G, NM_170733.3:c.*2235A>G, NM_170734.4:c.*2236A>G, NM_170734.3:c.*2235A>G, NM_001143816.2:c.*2236A>G, NM_001143816.1:c.*2235A>G, NM_001143811.2:c.*2236A>G, NM_001143811.1:c.*2235A>G, NM_001143814.2:c.*2236A>G, NM_001143814.1:c.*2235A>G, NM_001143810.2:c.*2236A>G, NM_001143810.1:c.*2235A>G, NM_001143813.2:c.*2236A>G, NM_001143813.1:c.*2235A>G, NM_001143812.2:c.*2236A>G, NM_001143812.1:c.*2235A>G, NM_001143809.2:c.*2236A>G, NM_001143809.1:c.*2235A>G, NM_001143808.2:c.*2236A>G, NM_001143808.1:c.*2235A>G, NM_001143807.2:c.*2236A>G, NM_001143807.1:c.*2235A>G, NM_001143806.1:c.*2235A>G, NM_001143805.1:c.*2235A>G, NM_001143815.1:c.*2235A>G

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