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Items: 1 to 20 of 715

1.

rs1487796765 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    T>A [Show Flanks]
    Chromosome:
    1:231626885 (GRCh38)
    1:231762631 (GRCh37)
    Canonical SPDI:
    NC_000001.11:231626884:T:A
    Gene:
    DISC1 (Varview), TSNAX-DISC1 (Varview)
    Functional Consequence:
    intron_variant,synonymous_variant,coding_sequence_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    A=0./0 (ALFA)
    A=0.000008/2 (TOPMED)
    A=0.000022/2 (GnomAD_exomes)
    HGVS:
    NC_000001.11:g.231626885T>A, NC_000001.10:g.231762631T>A, NG_011681.2:g.5071T>A, NM_018662.3:c.18T>A, NM_018662.2:c.18T>A, NM_001164537.2:c.18T>A, NM_001164537.1:c.18T>A, NM_001012957.2:c.18T>A, NM_001012957.1:c.18T>A, NM_001164540.2:c.18T>A, NM_001164540.1:c.18T>A, NM_001164538.2:c.18T>A, NM_001164538.1:c.18T>A, NM_001164541.2:c.18T>A, NM_001164541.1:c.18T>A, NM_001164550.2:c.18T>A, NM_001164550.1:c.18T>A, NM_001164552.2:c.18T>A, NM_001164552.1:c.18T>A, NM_001164544.2:c.18T>A, NM_001164544.1:c.18T>A, NM_001164542.2:c.18T>A, NM_001164542.1:c.18T>A, NM_001164553.2:c.18T>A, NM_001164553.1:c.18T>A, NM_001164539.2:c.18T>A, NM_001164539.1:c.18T>A, NM_001012958.2:c.18T>A, NM_001012958.1:c.18T>A, NM_001164545.2:c.18T>A, NM_001164545.1:c.18T>A, NM_001164547.2:c.18T>A, NM_001164547.1:c.18T>A, NM_001164548.2:c.18T>A, NM_001164548.1:c.18T>A, NM_001164546.2:c.18T>A, NM_001164546.1:c.18T>A, NM_001164549.2:c.18T>A, NM_001164549.1:c.18T>A, NM_001012959.2:c.18T>A, NM_001012959.1:c.18T>A, NM_001164551.2:c.18T>A, NM_001164551.1:c.18T>A, NM_001164554.2:c.18T>A, NM_001164554.1:c.18T>A, NM_001164555.2:c.18T>A, NM_001164555.1:c.18T>A, NM_001164556.2:c.18T>A, NM_001164556.1:c.18T>A

    2.

    rs1486438784 [Homo sapiens]
      Variant type:
      SNV
      Alleles:
      G>A [Show Flanks]
      Chromosome:
      1:231694725 (GRCh38)
      1:231830471 (GRCh37)
      Canonical SPDI:
      NC_000001.11:231694724:G:A
      Gene:
      DISC1 (Varview), TSNAX-DISC1 (Varview)
      Functional Consequence:
      non_coding_transcript_variant,intron_variant,missense_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      A=0.000071/1 (ALFA)
      A=0.000004/1 (GnomAD_exomes)
      A=0.000008/2 (TOPMED)
      A=0.000014/2 (GnomAD)
      HGVS:
      NC_000001.11:g.231694725G>A, NC_000001.10:g.231830471G>A, NG_011681.2:g.72911G>A, NM_018662.3:c.967G>A, NM_018662.2:c.967G>A, NM_001164537.2:c.967G>A, NM_001164537.1:c.967G>A, NM_001012957.2:c.967G>A, NM_001012957.1:c.967G>A, NM_001164540.2:c.967G>A, NM_001164540.1:c.967G>A, NM_001164538.2:c.967G>A, NM_001164538.1:c.967G>A, NM_001164541.2:c.967G>A, NM_001164541.1:c.967G>A, NM_001164550.2:c.967G>A, NM_001164550.1:c.967G>A, NM_001164552.2:c.967G>A, NM_001164552.1:c.967G>A, NM_001164544.2:c.967G>A, NM_001164544.1:c.967G>A, NM_001164542.2:c.967G>A, NM_001164542.1:c.967G>A, NM_001164553.2:c.967G>A, NM_001164553.1:c.967G>A, NM_001164539.2:c.967G>A, NM_001164539.1:c.967G>A, NM_001012958.2:c.967G>A, NM_001012958.1:c.967G>A, NM_001164545.2:c.967G>A, NM_001164545.1:c.967G>A, NM_001164547.2:c.967G>A, NM_001164547.1:c.967G>A, NM_001164548.2:c.967G>A, NM_001164548.1:c.967G>A, NM_001164546.2:c.967G>A, NM_001164546.1:c.967G>A, NM_001164549.2:c.967G>A, NM_001164549.1:c.967G>A, NM_001012959.2:c.967G>A, NM_001012959.1:c.967G>A, NM_001164551.2:c.967G>A, NM_001164551.1:c.967G>A, NM_001164554.2:c.967G>A, NM_001164554.1:c.967G>A, NM_001164555.2:c.967G>A, NM_001164555.1:c.967G>A, NR_028393.1:n.1688G>A, NR_028394.1:n.1816G>A, NR_028395.1:n.1816G>A, NR_028396.1:n.1688G>A, NR_028397.1:n.1553G>A, NR_028398.1:n.1307G>A, NR_028399.1:n.1923G>A, NR_028400.1:n.1795G>A, NP_061132.2:p.Ala323Thr, NP_001158009.1:p.Ala323Thr, NP_001012975.1:p.Ala323Thr, NP_001158012.1:p.Ala323Thr, NP_001158010.1:p.Ala323Thr, NP_001158013.1:p.Ala323Thr, NP_001158022.1:p.Ala323Thr, NP_001158024.1:p.Ala323Thr, NP_001158016.1:p.Ala323Thr, NP_001158014.1:p.Ala323Thr, NP_001158025.1:p.Ala323Thr, NP_001158011.1:p.Ala323Thr, NP_001012976.1:p.Ala323Thr, NP_001158017.1:p.Ala323Thr, NP_001158019.1:p.Ala323Thr, NP_001158020.1:p.Ala323Thr, NP_001158018.1:p.Ala323Thr, NP_001158021.1:p.Ala323Thr, NP_001012977.1:p.Ala323Thr, NP_001158023.1:p.Ala323Thr, NP_001158026.1:p.Ala323Thr, NP_001158027.1:p.Ala323Thr

      3.

      rs1483308206 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        C>A,T [Show Flanks]
        Chromosome:
        1:231795264 (GRCh38)
        1:231931010 (GRCh37)
        Canonical SPDI:
        NC_000001.11:231795263:C:A,NC_000001.11:231795263:C:T
        Gene:
        DISC1 (Varview), TSNAX-DISC1 (Varview)
        Functional Consequence:
        missense_variant,intron_variant,non_coding_transcript_variant,coding_sequence_variant,genic_downstream_transcript_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0.000071/1 (ALFA)
        A=0.000004/1 (GnomAD_exomes)
        T=0.000007/1 (GnomAD)
        HGVS:
        NC_000001.11:g.231795264C>A, NC_000001.11:g.231795264C>T, NC_000001.10:g.231931010C>A, NC_000001.10:g.231931010C>T, NG_011681.2:g.173450C>A, NG_011681.2:g.173450C>T, NM_018662.3:c.1657C>A, NM_018662.3:c.1657C>T, NM_018662.2:c.1657C>A, NM_018662.2:c.1657C>T, NM_001164537.2:c.1753C>A, NM_001164537.2:c.1753C>T, NM_001164537.1:c.1753C>A, NM_001164537.1:c.1753C>T, NM_001012957.2:c.1657C>A, NM_001012957.2:c.1657C>T, NM_001012957.1:c.1657C>A, NM_001012957.1:c.1657C>T, NM_001164540.2:c.1291C>A, NM_001164540.2:c.1291C>T, NM_001164540.1:c.1291C>A, NM_001164540.1:c.1291C>T, NM_001164538.2:c.1657C>A, NM_001164538.2:c.1657C>T, NM_001164538.1:c.1657C>A, NM_001164538.1:c.1657C>T, NM_001164541.2:c.1657C>A, NM_001164541.2:c.1657C>T, NM_001164541.1:c.1657C>A, NM_001164541.1:c.1657C>T, NM_001164544.2:c.1657C>A, NM_001164544.2:c.1657C>T, NM_001164544.1:c.1657C>A, NM_001164544.1:c.1657C>T, NM_001164542.2:c.1657C>A, NM_001164542.2:c.1657C>T, NM_001164542.1:c.1657C>A, NM_001164542.1:c.1657C>T, NM_001164539.2:c.1657C>A, NM_001164539.2:c.1657C>T, NM_001164539.1:c.1657C>A, NM_001164539.1:c.1657C>T, NM_001164545.2:c.1657C>A, NM_001164545.2:c.1657C>T, NM_001164545.1:c.1657C>A, NM_001164545.1:c.1657C>T, NM_001012959.2:c.1657C>A, NM_001012959.2:c.1657C>T, NM_001012959.1:c.1657C>A, NM_001012959.1:c.1657C>T, NR_028394.1:n.2506C>A, NR_028394.1:n.2506C>T, NR_028395.1:n.2506C>A, NR_028395.1:n.2506C>T, NR_028396.1:n.2378C>A, NR_028396.1:n.2378C>T, NR_028397.1:n.2243C>A, NR_028397.1:n.2243C>T, NR_028398.1:n.1997C>A, NR_028398.1:n.1997C>T, NP_061132.2:p.Leu553Ile, NP_061132.2:p.Leu553Phe, NP_001158009.1:p.Leu585Ile, NP_001158009.1:p.Leu585Phe, NP_001012975.1:p.Leu553Ile, NP_001012975.1:p.Leu553Phe, NP_001158012.1:p.Leu431Ile, NP_001158012.1:p.Leu431Phe, NP_001158010.1:p.Leu553Ile, NP_001158010.1:p.Leu553Phe, NP_001158013.1:p.Leu553Ile, NP_001158013.1:p.Leu553Phe, NP_001158016.1:p.Leu553Ile, NP_001158016.1:p.Leu553Phe, NP_001158014.1:p.Leu553Ile, NP_001158014.1:p.Leu553Phe, NP_001158011.1:p.Leu553Ile, NP_001158011.1:p.Leu553Phe, NP_001158017.1:p.Leu553Ile, NP_001158017.1:p.Leu553Phe, NP_001012977.1:p.Leu553Ile, NP_001012977.1:p.Leu553Phe

        4.

        rs1482018226 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A [Show Flanks]
          Chromosome:
          1:231767237 (GRCh38)
          1:231902983 (GRCh37)
          Canonical SPDI:
          NC_000001.11:231767236:G:A
          Gene:
          DISC1 (Varview), TSNAX-DISC1 (Varview)
          Functional Consequence:
          missense_variant,intron_variant,non_coding_transcript_variant,coding_sequence_variant,genic_downstream_transcript_variant
          Validated:
          by frequency,by alfa
          MAF:
          A=0./0 (ALFA)
          A=0.000004/1 (GnomAD_exomes)
          HGVS:
          NC_000001.11:g.231767237G>A, NC_000001.10:g.231902983G>A, NG_011681.2:g.145423G>A, NM_018662.3:c.1366G>A, NM_018662.2:c.1366G>A, NM_001164537.2:c.1462G>A, NM_001164537.1:c.1462G>A, NM_001012957.2:c.1366G>A, NM_001012957.1:c.1366G>A, NM_001164538.2:c.1366G>A, NM_001164538.1:c.1366G>A, NM_001164541.2:c.1366G>A, NM_001164541.1:c.1366G>A, NM_001164544.2:c.1366G>A, NM_001164544.1:c.1366G>A, NM_001164542.2:c.1366G>A, NM_001164542.1:c.1366G>A, NM_001164539.2:c.1366G>A, NM_001164539.1:c.1366G>A, NM_001164545.2:c.1366G>A, NM_001164545.1:c.1366G>A, NM_001164547.2:c.1366G>A, NM_001164547.1:c.1366G>A, NM_001164548.2:c.1366G>A, NM_001164548.1:c.1366G>A, NM_001164546.2:c.1366G>A, NM_001164546.1:c.1366G>A, NM_001164549.2:c.1366G>A, NM_001164549.1:c.1366G>A, NM_001012959.2:c.1366G>A, NM_001012959.1:c.1366G>A, NM_001164556.2:c.316G>A, NM_001164556.1:c.316G>A, NR_028393.1:n.2087G>A, NR_028394.1:n.2215G>A, NR_028395.1:n.2215G>A, NR_028396.1:n.2087G>A, NR_028397.1:n.1952G>A, NR_028398.1:n.1706G>A, NP_061132.2:p.Asp456Asn, NP_001158009.1:p.Asp488Asn, NP_001012975.1:p.Asp456Asn, NP_001158010.1:p.Asp456Asn, NP_001158013.1:p.Asp456Asn, NP_001158016.1:p.Asp456Asn, NP_001158014.1:p.Asp456Asn, NP_001158011.1:p.Asp456Asn, NP_001158017.1:p.Asp456Asn, NP_001158019.1:p.Asp456Asn, NP_001158020.1:p.Asp456Asn, NP_001158018.1:p.Asp456Asn, NP_001158021.1:p.Asp456Asn, NP_001012977.1:p.Asp456Asn, NP_001158028.1:p.Asp106Asn

          5.

          rs1476611302 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>A [Show Flanks]
            Chromosome:
            1:232008867 (GRCh38)
            1:232144613 (GRCh37)
            Canonical SPDI:
            NC_000001.11:232008866:G:A
            Gene:
            DISC1 (Varview), TSNAX-DISC1 (Varview)
            Functional Consequence:
            missense_variant,synonymous_variant,3_prime_UTR_variant,non_coding_transcript_variant,coding_sequence_variant,genic_downstream_transcript_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            A=0./0 (ALFA)
            A=0.000004/1 (TOPMED)
            A=0.000007/1 (GnomAD)
            HGVS:

            6.

            rs1476384887 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              A>G [Show Flanks]
              Chromosome:
              1:231694749 (GRCh38)
              1:231830495 (GRCh37)
              Canonical SPDI:
              NC_000001.11:231694748:A:G
              Gene:
              DISC1 (Varview), TSNAX-DISC1 (Varview)
              Functional Consequence:
              non_coding_transcript_variant,intron_variant,coding_sequence_variant,missense_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              G=0.000031/1 (ALFA)
              G=0.000004/1 (GnomAD_exomes)
              G=0.000007/1 (GnomAD)
              G=0.000008/2 (TOPMED)
              HGVS:
              NC_000001.11:g.231694749A>G, NC_000001.10:g.231830495A>G, NG_011681.2:g.72935A>G, NM_018662.3:c.991A>G, NM_018662.2:c.991A>G, NM_001164537.2:c.991A>G, NM_001164537.1:c.991A>G, NM_001012957.2:c.991A>G, NM_001012957.1:c.991A>G, NM_001164540.2:c.991A>G, NM_001164540.1:c.991A>G, NM_001164538.2:c.991A>G, NM_001164538.1:c.991A>G, NM_001164541.2:c.991A>G, NM_001164541.1:c.991A>G, NM_001164550.2:c.991A>G, NM_001164550.1:c.991A>G, NM_001164552.2:c.991A>G, NM_001164552.1:c.991A>G, NM_001164544.2:c.991A>G, NM_001164544.1:c.991A>G, NM_001164542.2:c.991A>G, NM_001164542.1:c.991A>G, NM_001164553.2:c.991A>G, NM_001164553.1:c.991A>G, NM_001164539.2:c.991A>G, NM_001164539.1:c.991A>G, NM_001012958.2:c.991A>G, NM_001012958.1:c.991A>G, NM_001164545.2:c.991A>G, NM_001164545.1:c.991A>G, NM_001164547.2:c.991A>G, NM_001164547.1:c.991A>G, NM_001164548.2:c.991A>G, NM_001164548.1:c.991A>G, NM_001164546.2:c.991A>G, NM_001164546.1:c.991A>G, NM_001164549.2:c.991A>G, NM_001164549.1:c.991A>G, NM_001012959.2:c.991A>G, NM_001012959.1:c.991A>G, NM_001164551.2:c.991A>G, NM_001164551.1:c.991A>G, NM_001164554.2:c.991A>G, NM_001164554.1:c.991A>G, NM_001164555.2:c.991A>G, NM_001164555.1:c.991A>G, NR_028393.1:n.1712A>G, NR_028394.1:n.1840A>G, NR_028395.1:n.1840A>G, NR_028396.1:n.1712A>G, NR_028397.1:n.1577A>G, NR_028398.1:n.1331A>G, NR_028399.1:n.1947A>G, NR_028400.1:n.1819A>G, NP_061132.2:p.Arg331Gly, NP_001158009.1:p.Arg331Gly, NP_001012975.1:p.Arg331Gly, NP_001158012.1:p.Arg331Gly, NP_001158010.1:p.Arg331Gly, NP_001158013.1:p.Arg331Gly, NP_001158022.1:p.Arg331Gly, NP_001158024.1:p.Arg331Gly, NP_001158016.1:p.Arg331Gly, NP_001158014.1:p.Arg331Gly, NP_001158025.1:p.Arg331Gly, NP_001158011.1:p.Arg331Gly, NP_001012976.1:p.Arg331Gly, NP_001158017.1:p.Arg331Gly, NP_001158019.1:p.Arg331Gly, NP_001158020.1:p.Arg331Gly, NP_001158018.1:p.Arg331Gly, NP_001158021.1:p.Arg331Gly, NP_001012977.1:p.Arg331Gly, NP_001158023.1:p.Arg331Gly, NP_001158026.1:p.Arg331Gly, NP_001158027.1:p.Arg331Gly

              7.

              rs1474002143 [Homo sapiens]
                Variant type:
                SNV
                Alleles:
                C>T [Show Flanks]
                Chromosome:
                1:231694035 (GRCh38)
                1:231829781 (GRCh37)
                Canonical SPDI:
                NC_000001.11:231694034:C:T
                Gene:
                DISC1 (Varview), TSNAX-DISC1 (Varview)
                Functional Consequence:
                missense_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                T=0./0 (ALFA)
                T=0.000004/1 (GnomAD_exomes)
                T=0.000004/1 (TOPMED)
                HGVS:
                NC_000001.11:g.231694035C>T, NC_000001.10:g.231829781C>T, NG_011681.2:g.72221C>T, NM_018662.3:c.277C>T, NM_018662.2:c.277C>T, NM_001164537.2:c.277C>T, NM_001164537.1:c.277C>T, NM_001012957.2:c.277C>T, NM_001012957.1:c.277C>T, NM_001164540.2:c.277C>T, NM_001164540.1:c.277C>T, NM_001164538.2:c.277C>T, NM_001164538.1:c.277C>T, NM_001164541.2:c.277C>T, NM_001164541.1:c.277C>T, NM_001164550.2:c.277C>T, NM_001164550.1:c.277C>T, NM_001164552.2:c.277C>T, NM_001164552.1:c.277C>T, NM_001164544.2:c.277C>T, NM_001164544.1:c.277C>T, NM_001164542.2:c.277C>T, NM_001164542.1:c.277C>T, NM_001164553.2:c.277C>T, NM_001164553.1:c.277C>T, NM_001164539.2:c.277C>T, NM_001164539.1:c.277C>T, NM_001012958.2:c.277C>T, NM_001012958.1:c.277C>T, NM_001164545.2:c.277C>T, NM_001164545.1:c.277C>T, NM_001164547.2:c.277C>T, NM_001164547.1:c.277C>T, NM_001164548.2:c.277C>T, NM_001164548.1:c.277C>T, NM_001164546.2:c.277C>T, NM_001164546.1:c.277C>T, NM_001164549.2:c.277C>T, NM_001164549.1:c.277C>T, NM_001012959.2:c.277C>T, NM_001012959.1:c.277C>T, NM_001164551.2:c.277C>T, NM_001164551.1:c.277C>T, NM_001164554.2:c.277C>T, NM_001164554.1:c.277C>T, NM_001164555.2:c.277C>T, NM_001164555.1:c.277C>T, NR_028393.1:n.998C>T, NR_028394.1:n.1126C>T, NR_028395.1:n.1126C>T, NR_028396.1:n.998C>T, NR_028397.1:n.863C>T, NR_028398.1:n.617C>T, NR_028399.1:n.1233C>T, NR_028400.1:n.1105C>T, NP_061132.2:p.Leu93Phe, NP_001158009.1:p.Leu93Phe, NP_001012975.1:p.Leu93Phe, NP_001158012.1:p.Leu93Phe, NP_001158010.1:p.Leu93Phe, NP_001158013.1:p.Leu93Phe, NP_001158022.1:p.Leu93Phe, NP_001158024.1:p.Leu93Phe, NP_001158016.1:p.Leu93Phe, NP_001158014.1:p.Leu93Phe, NP_001158025.1:p.Leu93Phe, NP_001158011.1:p.Leu93Phe, NP_001012976.1:p.Leu93Phe, NP_001158017.1:p.Leu93Phe, NP_001158019.1:p.Leu93Phe, NP_001158020.1:p.Leu93Phe, NP_001158018.1:p.Leu93Phe, NP_001158021.1:p.Leu93Phe, NP_001012977.1:p.Leu93Phe, NP_001158023.1:p.Leu93Phe, NP_001158026.1:p.Leu93Phe, NP_001158027.1:p.Leu93Phe

                8.

                rs1469382298 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  ->GAGGCGGCGGC [Show Flanks]
                  Chromosome:
                  1:231693862 (GRCh38)
                  1:231829609 (GRCh37)
                  Canonical SPDI:
                  NC_000001.11:231693862:GAGGCGGCGGC:GAGGCGGCGGCGAGGCGGCGGC
                  Gene:
                  DISC1 (Varview), TSNAX-DISC1 (Varview)
                  Functional Consequence:
                  frameshift_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
                  Validated:
                  by cluster
                  HGVS:
                  NC_000001.11:g.231693863_231693873dup, NC_000001.10:g.231829609_231829619dup, NG_011681.2:g.72049_72059dup, NM_018662.3:c.105_115dup, NM_018662.2:c.105_115dup, NM_001164537.2:c.105_115dup, NM_001164537.1:c.105_115dup, NM_001012957.2:c.105_115dup, NM_001012957.1:c.105_115dup, NM_001164540.2:c.105_115dup, NM_001164540.1:c.105_115dup, NM_001164538.2:c.105_115dup, NM_001164538.1:c.105_115dup, NM_001164541.2:c.105_115dup, NM_001164541.1:c.105_115dup, NM_001164550.2:c.105_115dup, NM_001164550.1:c.105_115dup, NM_001164552.2:c.105_115dup, NM_001164552.1:c.105_115dup, NM_001164544.2:c.105_115dup, NM_001164544.1:c.105_115dup, NM_001164542.2:c.105_115dup, NM_001164542.1:c.105_115dup, NM_001164553.2:c.105_115dup, NM_001164553.1:c.105_115dup, NM_001164539.2:c.105_115dup, NM_001164539.1:c.105_115dup, NM_001012958.2:c.105_115dup, NM_001012958.1:c.105_115dup, NM_001164545.2:c.105_115dup, NM_001164545.1:c.105_115dup, NM_001164547.2:c.105_115dup, NM_001164547.1:c.105_115dup, NM_001164548.2:c.105_115dup, NM_001164548.1:c.105_115dup, NM_001164546.2:c.105_115dup, NM_001164546.1:c.105_115dup, NM_001164549.2:c.105_115dup, NM_001164549.1:c.105_115dup, NM_001012959.2:c.105_115dup, NM_001012959.1:c.105_115dup, NM_001164551.2:c.105_115dup, NM_001164551.1:c.105_115dup, NM_001164554.2:c.105_115dup, NM_001164554.1:c.105_115dup, NM_001164555.2:c.105_115dup, NM_001164555.1:c.105_115dup, NR_028393.1:n.826_836dup, NR_028394.1:n.954_964dup, NR_028395.1:n.954_964dup, NR_028396.1:n.826_836dup, NR_028397.1:n.691_701dup, NR_028398.1:n.445_455dup, NR_028399.1:n.1061_1071dup, NR_028400.1:n.933_943dup, NP_061132.2:p.Leu39fs, NP_001158009.1:p.Leu39fs, NP_001012975.1:p.Leu39fs, NP_001158012.1:p.Leu39fs, NP_001158010.1:p.Leu39fs, NP_001158013.1:p.Leu39fs, NP_001158022.1:p.Leu39fs, NP_001158024.1:p.Leu39fs, NP_001158016.1:p.Leu39fs, NP_001158014.1:p.Leu39fs, NP_001158025.1:p.Leu39fs, NP_001158011.1:p.Leu39fs, NP_001012976.1:p.Leu39fs, NP_001158017.1:p.Leu39fs, NP_001158019.1:p.Leu39fs, NP_001158020.1:p.Leu39fs, NP_001158018.1:p.Leu39fs, NP_001158021.1:p.Leu39fs, NP_001012977.1:p.Leu39fs, NP_001158023.1:p.Leu39fs, NP_001158026.1:p.Leu39fs, NP_001158027.1:p.Leu39fs

                  9.

                  rs1468456861 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    CTGGCTGTGG>- [Show Flanks]
                    Chromosome:
                    1:231694687 (GRCh38)
                    1:231830433 (GRCh37)
                    Canonical SPDI:
                    NC_000001.11:231694683:TGGCTGGCTGTGG:TGG
                    Gene:
                    DISC1 (Varview), TSNAX-DISC1 (Varview)
                    Functional Consequence:
                    frameshift_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    TGG=0./0 (ALFA)
                    -=0.000004/1 (TOPMED)
                    HGVS:
                    NC_000001.11:g.231694687_231694696del, NC_000001.10:g.231830433_231830442del, NG_011681.2:g.72873_72882del, NM_018662.3:c.929_938del, NM_018662.2:c.929_938del, NM_001164537.2:c.929_938del, NM_001164537.1:c.929_938del, NM_001012957.2:c.929_938del, NM_001012957.1:c.929_938del, NM_001164540.2:c.929_938del, NM_001164540.1:c.929_938del, NM_001164538.2:c.929_938del, NM_001164538.1:c.929_938del, NM_001164541.2:c.929_938del, NM_001164541.1:c.929_938del, NM_001164550.2:c.929_938del, NM_001164550.1:c.929_938del, NM_001164552.2:c.929_938del, NM_001164552.1:c.929_938del, NM_001164544.2:c.929_938del, NM_001164544.1:c.929_938del, NM_001164542.2:c.929_938del, NM_001164542.1:c.929_938del, NM_001164553.2:c.929_938del, NM_001164553.1:c.929_938del, NM_001164539.2:c.929_938del, NM_001164539.1:c.929_938del, NM_001012958.2:c.929_938del, NM_001012958.1:c.929_938del, NM_001164545.2:c.929_938del, NM_001164545.1:c.929_938del, NM_001164547.2:c.929_938del, NM_001164547.1:c.929_938del, NM_001164548.2:c.929_938del, NM_001164548.1:c.929_938del, NM_001164546.2:c.929_938del, NM_001164546.1:c.929_938del, NM_001164549.2:c.929_938del, NM_001164549.1:c.929_938del, NM_001012959.2:c.929_938del, NM_001012959.1:c.929_938del, NM_001164551.2:c.929_938del, NM_001164551.1:c.929_938del, NM_001164554.2:c.929_938del, NM_001164554.1:c.929_938del, NM_001164555.2:c.929_938del, NM_001164555.1:c.929_938del, NR_028393.1:n.1650_1659del, NR_028394.1:n.1778_1787del, NR_028395.1:n.1778_1787del, NR_028396.1:n.1650_1659del, NR_028397.1:n.1515_1524del, NR_028398.1:n.1269_1278del, NR_028399.1:n.1885_1894del, NR_028400.1:n.1757_1766del, NP_061132.2:p.Ala310fs, NP_001158009.1:p.Ala310fs, NP_001012975.1:p.Ala310fs, NP_001158012.1:p.Ala310fs, NP_001158010.1:p.Ala310fs, NP_001158013.1:p.Ala310fs, NP_001158022.1:p.Ala310fs, NP_001158024.1:p.Ala310fs, NP_001158016.1:p.Ala310fs, NP_001158014.1:p.Ala310fs, NP_001158025.1:p.Ala310fs, NP_001158011.1:p.Ala310fs, NP_001012976.1:p.Ala310fs, NP_001158017.1:p.Ala310fs, NP_001158019.1:p.Ala310fs, NP_001158020.1:p.Ala310fs, NP_001158018.1:p.Ala310fs, NP_001158021.1:p.Ala310fs, NP_001012977.1:p.Ala310fs, NP_001158023.1:p.Ala310fs, NP_001158026.1:p.Ala310fs, NP_001158027.1:p.Ala310fs

                    10.

                    rs1467388316 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      T>C [Show Flanks]
                      Chromosome:
                      1:231749956 (GRCh38)
                      1:231885702 (GRCh37)
                      Canonical SPDI:
                      NC_000001.11:231749955:T:C
                      Gene:
                      DISC1 (Varview), TSNAX-DISC1 (Varview)
                      Functional Consequence:
                      missense_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,3_prime_UTR_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      C=0.000031/1 (ALFA)
                      C=0.000004/1 (GnomAD_exomes)
                      HGVS:
                      NC_000001.11:g.231749956T>C, NC_000001.10:g.231885702T>C, NG_011681.2:g.128142T>C, NM_018662.3:c.1148T>C, NM_018662.2:c.1148T>C, NM_001164537.2:c.1244T>C, NM_001164537.1:c.1244T>C, NM_001012957.2:c.1148T>C, NM_001012957.1:c.1148T>C, NM_001164540.2:c.1148T>C, NM_001164540.1:c.1148T>C, NM_001164538.2:c.1148T>C, NM_001164538.1:c.1148T>C, NM_001164541.2:c.1148T>C, NM_001164541.1:c.1148T>C, NM_001164544.2:c.1148T>C, NM_001164544.1:c.1148T>C, NM_001164542.2:c.1148T>C, NM_001164542.1:c.1148T>C, NM_001164539.2:c.1148T>C, NM_001164539.1:c.1148T>C, NM_001164545.2:c.1148T>C, NM_001164545.1:c.1148T>C, NM_001164547.2:c.1148T>C, NM_001164547.1:c.1148T>C, NM_001164548.2:c.1148T>C, NM_001164548.1:c.1148T>C, NM_001164546.2:c.1148T>C, NM_001164546.1:c.1148T>C, NM_001164549.2:c.1148T>C, NM_001164549.1:c.1148T>C, NM_001012959.2:c.1148T>C, NM_001012959.1:c.1148T>C, NM_001164551.2:c.1148T>C, NM_001164551.1:c.1148T>C, NM_001164555.2:c.*7T>C, NM_001164555.1:c.*7T>C, NM_001164556.2:c.98T>C, NM_001164556.1:c.98T>C, NR_028393.1:n.1869T>C, NR_028394.1:n.1997T>C, NR_028395.1:n.1997T>C, NR_028396.1:n.1869T>C, NR_028397.1:n.1734T>C, NR_028398.1:n.1488T>C, NR_028400.1:n.1906T>C, NP_061132.2:p.Leu383Pro, NP_001158009.1:p.Leu415Pro, NP_001012975.1:p.Leu383Pro, NP_001158012.1:p.Leu383Pro, NP_001158010.1:p.Leu383Pro, NP_001158013.1:p.Leu383Pro, NP_001158016.1:p.Leu383Pro, NP_001158014.1:p.Leu383Pro, NP_001158011.1:p.Leu383Pro, NP_001158017.1:p.Leu383Pro, NP_001158019.1:p.Leu383Pro, NP_001158020.1:p.Leu383Pro, NP_001158018.1:p.Leu383Pro, NP_001158021.1:p.Leu383Pro, NP_001012977.1:p.Leu383Pro, NP_001158023.1:p.Leu383Pro, NP_001158028.1:p.Leu33Pro

                      11.

                      rs1467229857 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        A>G,T [Show Flanks]
                        Chromosome:
                        1:231694277 (GRCh38)
                        1:231830023 (GRCh37)
                        Canonical SPDI:
                        NC_000001.11:231694276:A:G,NC_000001.11:231694276:A:T
                        Gene:
                        DISC1 (Varview), TSNAX-DISC1 (Varview)
                        Functional Consequence:
                        non_coding_transcript_variant,synonymous_variant,coding_sequence_variant,intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0./0 (ALFA)
                        G=0.000004/1 (GnomAD_exomes)
                        T=0.000004/1 (TOPMED)
                        HGVS:
                        NC_000001.11:g.231694277A>G, NC_000001.11:g.231694277A>T, NC_000001.10:g.231830023A>G, NC_000001.10:g.231830023A>T, NG_011681.2:g.72463A>G, NG_011681.2:g.72463A>T, NM_018662.3:c.519A>G, NM_018662.3:c.519A>T, NM_018662.2:c.519A>G, NM_018662.2:c.519A>T, NM_001164537.2:c.519A>G, NM_001164537.2:c.519A>T, NM_001164537.1:c.519A>G, NM_001164537.1:c.519A>T, NM_001012957.2:c.519A>G, NM_001012957.2:c.519A>T, NM_001012957.1:c.519A>G, NM_001012957.1:c.519A>T, NM_001164540.2:c.519A>G, NM_001164540.2:c.519A>T, NM_001164540.1:c.519A>G, NM_001164540.1:c.519A>T, NM_001164538.2:c.519A>G, NM_001164538.2:c.519A>T, NM_001164538.1:c.519A>G, NM_001164538.1:c.519A>T, NM_001164541.2:c.519A>G, NM_001164541.2:c.519A>T, NM_001164541.1:c.519A>G, NM_001164541.1:c.519A>T, NM_001164550.2:c.519A>G, NM_001164550.2:c.519A>T, NM_001164550.1:c.519A>G, NM_001164550.1:c.519A>T, NM_001164552.2:c.519A>G, NM_001164552.2:c.519A>T, NM_001164552.1:c.519A>G, NM_001164552.1:c.519A>T, NM_001164544.2:c.519A>G, NM_001164544.2:c.519A>T, NM_001164544.1:c.519A>G, NM_001164544.1:c.519A>T, NM_001164542.2:c.519A>G, NM_001164542.2:c.519A>T, NM_001164542.1:c.519A>G, NM_001164542.1:c.519A>T, NM_001164553.2:c.519A>G, NM_001164553.2:c.519A>T, NM_001164553.1:c.519A>G, NM_001164553.1:c.519A>T, NM_001164539.2:c.519A>G, NM_001164539.2:c.519A>T, NM_001164539.1:c.519A>G, NM_001164539.1:c.519A>T, NM_001012958.2:c.519A>G, NM_001012958.2:c.519A>T, NM_001012958.1:c.519A>G, NM_001012958.1:c.519A>T, NM_001164545.2:c.519A>G, NM_001164545.2:c.519A>T, NM_001164545.1:c.519A>G, NM_001164545.1:c.519A>T, NM_001164547.2:c.519A>G, NM_001164547.2:c.519A>T, NM_001164547.1:c.519A>G, NM_001164547.1:c.519A>T, NM_001164548.2:c.519A>G, NM_001164548.2:c.519A>T, NM_001164548.1:c.519A>G, NM_001164548.1:c.519A>T, NM_001164546.2:c.519A>G, NM_001164546.2:c.519A>T, NM_001164546.1:c.519A>G, NM_001164546.1:c.519A>T, NM_001164549.2:c.519A>G, NM_001164549.2:c.519A>T, NM_001164549.1:c.519A>G, NM_001164549.1:c.519A>T, NM_001012959.2:c.519A>G, NM_001012959.2:c.519A>T, NM_001012959.1:c.519A>G, NM_001012959.1:c.519A>T, NM_001164551.2:c.519A>G, NM_001164551.2:c.519A>T, NM_001164551.1:c.519A>G, NM_001164551.1:c.519A>T, NM_001164554.2:c.519A>G, NM_001164554.2:c.519A>T, NM_001164554.1:c.519A>G, NM_001164554.1:c.519A>T, NM_001164555.2:c.519A>G, NM_001164555.2:c.519A>T, NM_001164555.1:c.519A>G, NM_001164555.1:c.519A>T, NR_028393.1:n.1240A>G, NR_028393.1:n.1240A>T, NR_028394.1:n.1368A>G, NR_028394.1:n.1368A>T, NR_028395.1:n.1368A>G, NR_028395.1:n.1368A>T, NR_028396.1:n.1240A>G, NR_028396.1:n.1240A>T, NR_028397.1:n.1105A>G, NR_028397.1:n.1105A>T, NR_028398.1:n.859A>G, NR_028398.1:n.859A>T, NR_028399.1:n.1475A>G, NR_028399.1:n.1475A>T, NR_028400.1:n.1347A>G, NR_028400.1:n.1347A>T

                        12.

                        rs1466619030 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          1:231800110 (GRCh38)
                          1:231935856 (GRCh37)
                          Canonical SPDI:
                          NC_000001.11:231800109:G:A
                          Gene:
                          DISC1 (Varview), TSNAX-DISC1 (Varview)
                          Functional Consequence:
                          synonymous_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0./0 (ALFA)
                          A=0.000004/1 (GnomAD_exomes)
                          A=0.000004/1 (TOPMED)
                          HGVS:

                          13.

                          rs1465110999 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            G>A [Show Flanks]
                            Chromosome:
                            1:231770975 (GRCh38)
                            1:231906721 (GRCh37)
                            Canonical SPDI:
                            NC_000001.11:231770974:G:A
                            Gene:
                            DISC1 (Varview), TSNAX-DISC1 (Varview)
                            Functional Consequence:
                            synonymous_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            A=0./0 (ALFA)
                            A=0.000007/1 (GnomAD)
                            HGVS:
                            NC_000001.11:g.231770975G>A, NC_000001.10:g.231906721G>A, NG_011681.2:g.149161G>A, NM_018662.3:c.1539G>A, NM_018662.2:c.1539G>A, NM_001164537.2:c.1635G>A, NM_001164537.1:c.1635G>A, NM_001012957.2:c.1539G>A, NM_001012957.1:c.1539G>A, NM_001164538.2:c.1539G>A, NM_001164538.1:c.1539G>A, NM_001164541.2:c.1539G>A, NM_001164541.1:c.1539G>A, NM_001164544.2:c.1539G>A, NM_001164544.1:c.1539G>A, NM_001164542.2:c.1539G>A, NM_001164542.1:c.1539G>A, NM_001164539.2:c.1539G>A, NM_001164539.1:c.1539G>A, NM_001164545.2:c.1539G>A, NM_001164545.1:c.1539G>A, NM_001164547.2:c.1539G>A, NM_001164547.1:c.1539G>A, NM_001164548.2:c.1539G>A, NM_001164548.1:c.1539G>A, NM_001164546.2:c.1539G>A, NM_001164546.1:c.1539G>A, NM_001164549.2:c.1539G>A, NM_001164549.1:c.1539G>A, NM_001012959.2:c.1539G>A, NM_001012959.1:c.1539G>A, NM_001164556.2:c.489G>A, NM_001164556.1:c.489G>A, NR_028393.1:n.2260G>A, NR_028394.1:n.2388G>A, NR_028395.1:n.2388G>A, NR_028396.1:n.2260G>A, NR_028397.1:n.2125G>A, NR_028398.1:n.1879G>A

                            14.

                            rs1464491607 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              C>A [Show Flanks]
                              Chromosome:
                              1:231750014 (GRCh38)
                              1:231885760 (GRCh37)
                              Canonical SPDI:
                              NC_000001.11:231750013:C:A
                              Gene:
                              DISC1 (Varview), TSNAX-DISC1 (Varview)
                              Functional Consequence:
                              missense_variant,genic_downstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,3_prime_UTR_variant
                              Validated:
                              by frequency
                              MAF:
                              A=0.000004/1 (GnomAD_exomes)
                              HGVS:
                              NC_000001.11:g.231750014C>A, NC_000001.10:g.231885760C>A, NG_011681.2:g.128200C>A, NM_018662.3:c.1206C>A, NM_018662.2:c.1206C>A, NM_001164537.2:c.1302C>A, NM_001164537.1:c.1302C>A, NM_001012957.2:c.1206C>A, NM_001012957.1:c.1206C>A, NM_001164540.2:c.1206C>A, NM_001164540.1:c.1206C>A, NM_001164538.2:c.1206C>A, NM_001164538.1:c.1206C>A, NM_001164541.2:c.1206C>A, NM_001164541.1:c.1206C>A, NM_001164544.2:c.1206C>A, NM_001164544.1:c.1206C>A, NM_001164542.2:c.1206C>A, NM_001164542.1:c.1206C>A, NM_001164539.2:c.1206C>A, NM_001164539.1:c.1206C>A, NM_001164545.2:c.1206C>A, NM_001164545.1:c.1206C>A, NM_001164547.2:c.1206C>A, NM_001164547.1:c.1206C>A, NM_001164548.2:c.1206C>A, NM_001164548.1:c.1206C>A, NM_001164546.2:c.1206C>A, NM_001164546.1:c.1206C>A, NM_001164549.2:c.1206C>A, NM_001164549.1:c.1206C>A, NM_001012959.2:c.1206C>A, NM_001012959.1:c.1206C>A, NM_001164551.2:c.1206C>A, NM_001164551.1:c.1206C>A, NM_001164555.2:c.*65C>A, NM_001164555.1:c.*65C>A, NM_001164556.2:c.156C>A, NM_001164556.1:c.156C>A, NR_028393.1:n.1927C>A, NR_028394.1:n.2055C>A, NR_028395.1:n.2055C>A, NR_028396.1:n.1927C>A, NR_028397.1:n.1792C>A, NR_028398.1:n.1546C>A, NR_028400.1:n.1964C>A, NP_061132.2:p.Ser402Arg, NP_001158009.1:p.Ser434Arg, NP_001012975.1:p.Ser402Arg, NP_001158012.1:p.Ser402Arg, NP_001158010.1:p.Ser402Arg, NP_001158013.1:p.Ser402Arg, NP_001158016.1:p.Ser402Arg, NP_001158014.1:p.Ser402Arg, NP_001158011.1:p.Ser402Arg, NP_001158017.1:p.Ser402Arg, NP_001158019.1:p.Ser402Arg, NP_001158020.1:p.Ser402Arg, NP_001158018.1:p.Ser402Arg, NP_001158021.1:p.Ser402Arg, NP_001012977.1:p.Ser402Arg, NP_001158023.1:p.Ser402Arg, NP_001158028.1:p.Ser52Arg

                              15.

                              rs1463414572 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>T [Show Flanks]
                                Chromosome:
                                1:231694678 (GRCh38)
                                1:231830424 (GRCh37)
                                Canonical SPDI:
                                NC_000001.11:231694677:C:T
                                Gene:
                                DISC1 (Varview), TSNAX-DISC1 (Varview)
                                Functional Consequence:
                                non_coding_transcript_variant,missense_variant,coding_sequence_variant,intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                T=0.000028/1 (ALFA)
                                T=0.000023/6 (TOPMED)
                                T=0.000036/5 (GnomAD)
                                HGVS:
                                NC_000001.11:g.231694678C>T, NC_000001.10:g.231830424C>T, NG_011681.2:g.72864C>T, NM_018662.3:c.920C>T, NM_018662.2:c.920C>T, NM_001164537.2:c.920C>T, NM_001164537.1:c.920C>T, NM_001012957.2:c.920C>T, NM_001012957.1:c.920C>T, NM_001164540.2:c.920C>T, NM_001164540.1:c.920C>T, NM_001164538.2:c.920C>T, NM_001164538.1:c.920C>T, NM_001164541.2:c.920C>T, NM_001164541.1:c.920C>T, NM_001164550.2:c.920C>T, NM_001164550.1:c.920C>T, NM_001164552.2:c.920C>T, NM_001164552.1:c.920C>T, NM_001164544.2:c.920C>T, NM_001164544.1:c.920C>T, NM_001164542.2:c.920C>T, NM_001164542.1:c.920C>T, NM_001164553.2:c.920C>T, NM_001164553.1:c.920C>T, NM_001164539.2:c.920C>T, NM_001164539.1:c.920C>T, NM_001012958.2:c.920C>T, NM_001012958.1:c.920C>T, NM_001164545.2:c.920C>T, NM_001164545.1:c.920C>T, NM_001164547.2:c.920C>T, NM_001164547.1:c.920C>T, NM_001164548.2:c.920C>T, NM_001164548.1:c.920C>T, NM_001164546.2:c.920C>T, NM_001164546.1:c.920C>T, NM_001164549.2:c.920C>T, NM_001164549.1:c.920C>T, NM_001012959.2:c.920C>T, NM_001012959.1:c.920C>T, NM_001164551.2:c.920C>T, NM_001164551.1:c.920C>T, NM_001164554.2:c.920C>T, NM_001164554.1:c.920C>T, NM_001164555.2:c.920C>T, NM_001164555.1:c.920C>T, NR_028393.1:n.1641C>T, NR_028394.1:n.1769C>T, NR_028395.1:n.1769C>T, NR_028396.1:n.1641C>T, NR_028397.1:n.1506C>T, NR_028398.1:n.1260C>T, NR_028399.1:n.1876C>T, NR_028400.1:n.1748C>T, NP_061132.2:p.Pro307Leu, NP_001158009.1:p.Pro307Leu, NP_001012975.1:p.Pro307Leu, NP_001158012.1:p.Pro307Leu, NP_001158010.1:p.Pro307Leu, NP_001158013.1:p.Pro307Leu, NP_001158022.1:p.Pro307Leu, NP_001158024.1:p.Pro307Leu, NP_001158016.1:p.Pro307Leu, NP_001158014.1:p.Pro307Leu, NP_001158025.1:p.Pro307Leu, NP_001158011.1:p.Pro307Leu, NP_001012976.1:p.Pro307Leu, NP_001158017.1:p.Pro307Leu, NP_001158019.1:p.Pro307Leu, NP_001158020.1:p.Pro307Leu, NP_001158018.1:p.Pro307Leu, NP_001158021.1:p.Pro307Leu, NP_001012977.1:p.Pro307Leu, NP_001158023.1:p.Pro307Leu, NP_001158026.1:p.Pro307Leu, NP_001158027.1:p.Pro307Leu

                                16.

                                rs1461578163 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>A [Show Flanks]
                                  Chromosome:
                                  1:231694130 (GRCh38)
                                  1:231829876 (GRCh37)
                                  Canonical SPDI:
                                  NC_000001.11:231694129:T:A
                                  Gene:
                                  DISC1 (Varview), TSNAX-DISC1 (Varview)
                                  Functional Consequence:
                                  non_coding_transcript_variant,synonymous_variant,coding_sequence_variant,intron_variant
                                  Validated:
                                  by frequency
                                  MAF:
                                  A=0.000004/1 (GnomAD_exomes)
                                  HGVS:
                                  NC_000001.11:g.231694130T>A, NC_000001.10:g.231829876T>A, NG_011681.2:g.72316T>A, NM_018662.3:c.372T>A, NM_018662.2:c.372T>A, NM_001164537.2:c.372T>A, NM_001164537.1:c.372T>A, NM_001012957.2:c.372T>A, NM_001012957.1:c.372T>A, NM_001164540.2:c.372T>A, NM_001164540.1:c.372T>A, NM_001164538.2:c.372T>A, NM_001164538.1:c.372T>A, NM_001164541.2:c.372T>A, NM_001164541.1:c.372T>A, NM_001164550.2:c.372T>A, NM_001164550.1:c.372T>A, NM_001164552.2:c.372T>A, NM_001164552.1:c.372T>A, NM_001164544.2:c.372T>A, NM_001164544.1:c.372T>A, NM_001164542.2:c.372T>A, NM_001164542.1:c.372T>A, NM_001164553.2:c.372T>A, NM_001164553.1:c.372T>A, NM_001164539.2:c.372T>A, NM_001164539.1:c.372T>A, NM_001012958.2:c.372T>A, NM_001012958.1:c.372T>A, NM_001164545.2:c.372T>A, NM_001164545.1:c.372T>A, NM_001164547.2:c.372T>A, NM_001164547.1:c.372T>A, NM_001164548.2:c.372T>A, NM_001164548.1:c.372T>A, NM_001164546.2:c.372T>A, NM_001164546.1:c.372T>A, NM_001164549.2:c.372T>A, NM_001164549.1:c.372T>A, NM_001012959.2:c.372T>A, NM_001012959.1:c.372T>A, NM_001164551.2:c.372T>A, NM_001164551.1:c.372T>A, NM_001164554.2:c.372T>A, NM_001164554.1:c.372T>A, NM_001164555.2:c.372T>A, NM_001164555.1:c.372T>A, NR_028393.1:n.1093T>A, NR_028394.1:n.1221T>A, NR_028395.1:n.1221T>A, NR_028396.1:n.1093T>A, NR_028397.1:n.958T>A, NR_028398.1:n.712T>A, NR_028399.1:n.1328T>A, NR_028400.1:n.1200T>A

                                  17.

                                  rs1456743930 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    A>G [Show Flanks]
                                    Chromosome:
                                    1:231795291 (GRCh38)
                                    1:231931037 (GRCh37)
                                    Canonical SPDI:
                                    NC_000001.11:231795290:A:G
                                    Gene:
                                    DISC1 (Varview), TSNAX-DISC1 (Varview)
                                    Functional Consequence:
                                    coding_sequence_variant,non_coding_transcript_variant,intron_variant,missense_variant,genic_downstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    G=0./0 (ALFA)
                                    G=0.000007/1 (GnomAD)
                                    G=0.000008/2 (GnomAD_exomes)
                                    G=0.000008/2 (TOPMED)
                                    HGVS:
                                    NC_000001.11:g.231795291A>G, NC_000001.10:g.231931037A>G, NG_011681.2:g.173477A>G, NM_018662.3:c.1684A>G, NM_018662.2:c.1684A>G, NM_001164537.2:c.1780A>G, NM_001164537.1:c.1780A>G, NM_001012957.2:c.1684A>G, NM_001012957.1:c.1684A>G, NM_001164540.2:c.1318A>G, NM_001164540.1:c.1318A>G, NM_001164538.2:c.1684A>G, NM_001164538.1:c.1684A>G, NM_001164541.2:c.1684A>G, NM_001164541.1:c.1684A>G, NM_001164544.2:c.1684A>G, NM_001164544.1:c.1684A>G, NM_001164542.2:c.1684A>G, NM_001164542.1:c.1684A>G, NM_001164539.2:c.1684A>G, NM_001164539.1:c.1684A>G, NM_001164545.2:c.1684A>G, NM_001164545.1:c.1684A>G, NM_001012959.2:c.1684A>G, NM_001012959.1:c.1684A>G, NR_028394.1:n.2533A>G, NR_028395.1:n.2533A>G, NR_028396.1:n.2405A>G, NR_028397.1:n.2270A>G, NR_028398.1:n.2024A>G, NP_061132.2:p.Thr562Ala, NP_001158009.1:p.Thr594Ala, NP_001012975.1:p.Thr562Ala, NP_001158012.1:p.Thr440Ala, NP_001158010.1:p.Thr562Ala, NP_001158013.1:p.Thr562Ala, NP_001158016.1:p.Thr562Ala, NP_001158014.1:p.Thr562Ala, NP_001158011.1:p.Thr562Ala, NP_001158017.1:p.Thr562Ala, NP_001012977.1:p.Thr562Ala

                                    18.

                                    rs1455131842 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>T [Show Flanks]
                                      Chromosome:
                                      1:231770946 (GRCh38)
                                      1:231906692 (GRCh37)
                                      Canonical SPDI:
                                      NC_000001.11:231770945:C:T
                                      Gene:
                                      DISC1 (Varview), TSNAX-DISC1 (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,non_coding_transcript_variant,intron_variant,synonymous_variant,genic_downstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      T=0./0 (ALFA)
                                      T=0.000008/2 (TOPMED)
                                      HGVS:
                                      NC_000001.11:g.231770946C>T, NC_000001.10:g.231906692C>T, NG_011681.2:g.149132C>T, NM_018662.3:c.1510C>T, NM_018662.2:c.1510C>T, NM_001164537.2:c.1606C>T, NM_001164537.1:c.1606C>T, NM_001012957.2:c.1510C>T, NM_001012957.1:c.1510C>T, NM_001164538.2:c.1510C>T, NM_001164538.1:c.1510C>T, NM_001164541.2:c.1510C>T, NM_001164541.1:c.1510C>T, NM_001164544.2:c.1510C>T, NM_001164544.1:c.1510C>T, NM_001164542.2:c.1510C>T, NM_001164542.1:c.1510C>T, NM_001164539.2:c.1510C>T, NM_001164539.1:c.1510C>T, NM_001164545.2:c.1510C>T, NM_001164545.1:c.1510C>T, NM_001164547.2:c.1510C>T, NM_001164547.1:c.1510C>T, NM_001164548.2:c.1510C>T, NM_001164548.1:c.1510C>T, NM_001164546.2:c.1510C>T, NM_001164546.1:c.1510C>T, NM_001164549.2:c.1510C>T, NM_001164549.1:c.1510C>T, NM_001012959.2:c.1510C>T, NM_001012959.1:c.1510C>T, NM_001164556.2:c.460C>T, NM_001164556.1:c.460C>T, NR_028393.1:n.2231C>T, NR_028394.1:n.2359C>T, NR_028395.1:n.2359C>T, NR_028396.1:n.2231C>T, NR_028397.1:n.2096C>T, NR_028398.1:n.1850C>T

                                      19.

                                      rs1452775697 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>T [Show Flanks]
                                        Chromosome:
                                        1:231694294 (GRCh38)
                                        1:231830040 (GRCh37)
                                        Canonical SPDI:
                                        NC_000001.11:231694293:C:T
                                        Gene:
                                        DISC1 (Varview), TSNAX-DISC1 (Varview)
                                        Functional Consequence:
                                        coding_sequence_variant,intron_variant,missense_variant,non_coding_transcript_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        T=0.000047/1 (ALFA)
                                        T=0.000004/1 (GnomAD_exomes)
                                        HGVS:
                                        NC_000001.11:g.231694294C>T, NC_000001.10:g.231830040C>T, NG_011681.2:g.72480C>T, NM_018662.3:c.536C>T, NM_018662.2:c.536C>T, NM_001164537.2:c.536C>T, NM_001164537.1:c.536C>T, NM_001012957.2:c.536C>T, NM_001012957.1:c.536C>T, NM_001164540.2:c.536C>T, NM_001164540.1:c.536C>T, NM_001164538.2:c.536C>T, NM_001164538.1:c.536C>T, NM_001164541.2:c.536C>T, NM_001164541.1:c.536C>T, NM_001164550.2:c.536C>T, NM_001164550.1:c.536C>T, NM_001164552.2:c.536C>T, NM_001164552.1:c.536C>T, NM_001164544.2:c.536C>T, NM_001164544.1:c.536C>T, NM_001164542.2:c.536C>T, NM_001164542.1:c.536C>T, NM_001164553.2:c.536C>T, NM_001164553.1:c.536C>T, NM_001164539.2:c.536C>T, NM_001164539.1:c.536C>T, NM_001012958.2:c.536C>T, NM_001012958.1:c.536C>T, NM_001164545.2:c.536C>T, NM_001164545.1:c.536C>T, NM_001164547.2:c.536C>T, NM_001164547.1:c.536C>T, NM_001164548.2:c.536C>T, NM_001164548.1:c.536C>T, NM_001164546.2:c.536C>T, NM_001164546.1:c.536C>T, NM_001164549.2:c.536C>T, NM_001164549.1:c.536C>T, NM_001012959.2:c.536C>T, NM_001012959.1:c.536C>T, NM_001164551.2:c.536C>T, NM_001164551.1:c.536C>T, NM_001164554.2:c.536C>T, NM_001164554.1:c.536C>T, NM_001164555.2:c.536C>T, NM_001164555.1:c.536C>T, NR_028393.1:n.1257C>T, NR_028394.1:n.1385C>T, NR_028395.1:n.1385C>T, NR_028396.1:n.1257C>T, NR_028397.1:n.1122C>T, NR_028398.1:n.876C>T, NR_028399.1:n.1492C>T, NR_028400.1:n.1364C>T, NP_061132.2:p.Ser179Leu, NP_001158009.1:p.Ser179Leu, NP_001012975.1:p.Ser179Leu, NP_001158012.1:p.Ser179Leu, NP_001158010.1:p.Ser179Leu, NP_001158013.1:p.Ser179Leu, NP_001158022.1:p.Ser179Leu, NP_001158024.1:p.Ser179Leu, NP_001158016.1:p.Ser179Leu, NP_001158014.1:p.Ser179Leu, NP_001158025.1:p.Ser179Leu, NP_001158011.1:p.Ser179Leu, NP_001012976.1:p.Ser179Leu, NP_001158017.1:p.Ser179Leu, NP_001158019.1:p.Ser179Leu, NP_001158020.1:p.Ser179Leu, NP_001158018.1:p.Ser179Leu, NP_001158021.1:p.Ser179Leu, NP_001012977.1:p.Ser179Leu, NP_001158023.1:p.Ser179Leu, NP_001158026.1:p.Ser179Leu, NP_001158027.1:p.Ser179Leu

                                        20.

                                        rs1452642173 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>A,C [Show Flanks]
                                          Chromosome:
                                          1:231701970 (GRCh38)
                                          1:231837716 (GRCh37)
                                          Canonical SPDI:
                                          NC_000001.11:231701969:T:A,NC_000001.11:231701969:T:C
                                          Gene:
                                          DISC1 (Varview), TSNAX-DISC1 (Varview)
                                          Functional Consequence:
                                          coding_sequence_variant,non_coding_transcript_variant,intron_variant,synonymous_variant,missense_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          C=0./0 (ALFA)
                                          HGVS:
                                          NC_000001.11:g.231701970T>A, NC_000001.11:g.231701970T>C, NC_000001.10:g.231837716T>A, NC_000001.10:g.231837716T>C, NG_011681.2:g.80156T>A, NG_011681.2:g.80156T>C, NM_018662.3:c.1063T>A, NM_018662.3:c.1063T>C, NM_018662.2:c.1063T>A, NM_018662.2:c.1063T>C, NM_001164537.2:c.1063T>A, NM_001164537.2:c.1063T>C, NM_001164537.1:c.1063T>A, NM_001164537.1:c.1063T>C, NM_001012957.2:c.1063T>A, NM_001012957.2:c.1063T>C, NM_001012957.1:c.1063T>A, NM_001012957.1:c.1063T>C, NM_001164540.2:c.1063T>A, NM_001164540.2:c.1063T>C, NM_001164540.1:c.1063T>A, NM_001164540.1:c.1063T>C, NM_001164538.2:c.1063T>A, NM_001164538.2:c.1063T>C, NM_001164538.1:c.1063T>A, NM_001164538.1:c.1063T>C, NM_001164541.2:c.1063T>A, NM_001164541.2:c.1063T>C, NM_001164541.1:c.1063T>A, NM_001164541.1:c.1063T>C, NM_001164550.2:c.1063T>A, NM_001164550.2:c.1063T>C, NM_001164550.1:c.1063T>A, NM_001164550.1:c.1063T>C, NM_001164552.2:c.1063T>A, NM_001164552.2:c.1063T>C, NM_001164552.1:c.1063T>A, NM_001164552.1:c.1063T>C, NM_001164544.2:c.1063T>A, NM_001164544.2:c.1063T>C, NM_001164544.1:c.1063T>A, NM_001164544.1:c.1063T>C, NM_001164542.2:c.1063T>A, NM_001164542.2:c.1063T>C, NM_001164542.1:c.1063T>A, NM_001164542.1:c.1063T>C, NM_001164553.2:c.1063T>A, NM_001164553.2:c.1063T>C, NM_001164553.1:c.1063T>A, NM_001164553.1:c.1063T>C, NM_001164539.2:c.1063T>A, NM_001164539.2:c.1063T>C, NM_001164539.1:c.1063T>A, NM_001164539.1:c.1063T>C, NM_001164545.2:c.1063T>A, NM_001164545.2:c.1063T>C, NM_001164545.1:c.1063T>A, NM_001164545.1:c.1063T>C, NM_001164547.2:c.1063T>A, NM_001164547.2:c.1063T>C, NM_001164547.1:c.1063T>A, NM_001164547.1:c.1063T>C, NM_001164548.2:c.1063T>A, NM_001164548.2:c.1063T>C, NM_001164548.1:c.1063T>A, NM_001164548.1:c.1063T>C, NM_001164546.2:c.1063T>A, NM_001164546.2:c.1063T>C, NM_001164546.1:c.1063T>A, NM_001164546.1:c.1063T>C, NM_001164549.2:c.1063T>A, NM_001164549.2:c.1063T>C, NM_001164549.1:c.1063T>A, NM_001164549.1:c.1063T>C, NM_001012959.2:c.1063T>A, NM_001012959.2:c.1063T>C, NM_001012959.1:c.1063T>A, NM_001012959.1:c.1063T>C, NM_001164551.2:c.1063T>A, NM_001164551.2:c.1063T>C, NM_001164551.1:c.1063T>A, NM_001164551.1:c.1063T>C, NM_001164554.2:c.1063T>A, NM_001164554.2:c.1063T>C, NM_001164554.1:c.1063T>A, NM_001164554.1:c.1063T>C, NR_028393.1:n.1784T>A, NR_028393.1:n.1784T>C, NR_028394.1:n.1912T>A, NR_028394.1:n.1912T>C, NR_028395.1:n.1912T>A, NR_028395.1:n.1912T>C, NR_028396.1:n.1784T>A, NR_028396.1:n.1784T>C, NR_028397.1:n.1649T>A, NR_028397.1:n.1649T>C, NR_028398.1:n.1403T>A, NR_028398.1:n.1403T>C, NR_028399.1:n.2019T>A, NR_028399.1:n.2019T>C, NM_025068.1:c.*287T>A, NM_025068.1:c.*287T>C, NM_001039383.1:c.*287T>A, NM_001039383.1:c.*287T>C, NM_001012992.1:c.*287T>A, NM_001012992.1:c.*287T>C, NP_061132.2:p.Leu355Ile, NP_001158009.1:p.Leu355Ile, NP_001012975.1:p.Leu355Ile, NP_001158012.1:p.Leu355Ile, NP_001158010.1:p.Leu355Ile, NP_001158013.1:p.Leu355Ile, NP_001158022.1:p.Leu355Ile, NP_001158024.1:p.Leu355Ile, NP_001158016.1:p.Leu355Ile, NP_001158014.1:p.Leu355Ile, NP_001158025.1:p.Leu355Ile, NP_001158011.1:p.Leu355Ile, NP_001158017.1:p.Leu355Ile, NP_001158019.1:p.Leu355Ile, NP_001158020.1:p.Leu355Ile, NP_001158018.1:p.Leu355Ile, NP_001158021.1:p.Leu355Ile, NP_001012977.1:p.Leu355Ile, NP_001158023.1:p.Leu355Ile, NP_001158026.1:p.Leu355Ile

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