Schema for snpArrayIlluminaHumanCytoSNP_12
  Database: hg18    Primary Table: snpArrayIlluminaHumanCytoSNP_12    Row Count: 302,402   Data last updated: 2010-03-22
Format description: Illumina 300K SNP Array
On download server: MariaDB table dump directory
fieldexampleSQL type info description
bin 590int(10) unsigned range For browser speedup
chrom chr1varchar(255) values Reference sequence chromosome or scaffold
chromStart 742428int(10) unsigned range Start position in chrom
chromEnd 742429int(10) unsigned range End position in chrom
name rs3094315varchar(255) values Identifier
score 0int(10) unsigned range Not used
strand -char(1) values Strand: +, - or ?
observed C/Tblob values Observed alleles

Connected Tables and Joining Fields
        hg18.gwasCatalog.name (via snpArrayIlluminaHumanCytoSNP_12.name)
      hg18.snp130.name (via snpArrayIlluminaHumanCytoSNP_12.name)
      hg18.snp130CodingDbSnp.name (via snpArrayIlluminaHumanCytoSNP_12.name)
      hg18.snp130Exceptions.name (via snpArrayIlluminaHumanCytoSNP_12.name)
      hg18.snp130OrthoPt2Pa2Rm2.name (via snpArrayIlluminaHumanCytoSNP_12.name)
      hg18.snp130Seq.acc (via snpArrayIlluminaHumanCytoSNP_12.name)
      hg18.snpArrayIlluminaHuman660W_Quad.name (via snpArrayIlluminaHumanCytoSNP_12.name)
      hg18.snpArrayIlluminaHumanOmni1_Quad.name (via snpArrayIlluminaHumanCytoSNP_12.name)

Sample Rows
 
binchromchromStartchromEndnamescorestrandobserved
590chr1742428742429rs30943150-C/T
590chr1743403743404rs20738130-C/T
590chr1760078760079rs29050400-C/T
590chr1766408766409rs121248190+A/G
590chr1771120771121rs29803140-A/C
590chr1781715781716rs66844870+A/G
591chr1789325789326rs42457560+C/T
591chr1798631798632rs120863110+A/G
591chr1806181806182rs39670010-A/G
591chr1806479806480rs133030770+A/G

Note: all start coordinates in our database are 0-based, not 1-based. See explanation here.