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bdi12203-sup-0001-FigureS1.docWord document33K

Figure S1. The introns and exons of the different splice variants of the ANK3 gene are shown, along with the genomic regions of the gene that were analysed for variant selection. The locations of the variants detected by sequencing are shown, as are the variants that were selected for genotyping in the full case control sample.

bdi12203-sup-0002-FigureS2.docWord document50K

Figure S2. The introns and exons of the different splice variants of the CACNA1C gene are shown, along with the genomic regions of the gene that were analysed for variant selection. The locations of the variants detected by sequencing are shown, as are the variants that were selected for genotyping in the full case–control sample.

bdi12203-sup-0003-TableS1.xlsapplication/msexcel63K

Table S1. Variants identified using the Knome VARIANTS software (Knome). VAF = variant allele(s) frequency.

bdi12203-sup-0004-TableS2.xlsapplication/msexcel30K

Table S2. Allele-specific primers designed using Primer Picker (KBiosciences) for genotyping.

bdi12203-sup-0005-TableS3.xlsxapplication/msexcel18K

Table S3. Next Generation Sequencing Control information.

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