Submitter Handle ILLUMINA Submitter SNP ID HumanOmniExpressExome-8v1_A_rs1205-131_T_R_1908813127 RefSNP(rs#) rs1205 Submitted Batch ID HumanOmniExpressExome-8v1_A Submitted Date May 31, 2013 Publication Cited N.D. First entry to dbSNP May 31 2013 12:00:00:000AM Resource Links Submitted Gene Name N.D Submitted Gene ID N.D. Submitted SNP Synonyms N.D Submitted linkout N.D Assay Species Homo sapiens Molecular Type Genomic Method ILLUMINA-CHIP Ascertainment Samplesize 2 Population N.D. Allele Observed Allele C/T Ancestral Allele N.D. Allele Origin N/A SNP Class SNV CpG Code N.D. Validation Validation Status Not Validated HWE Goodness of Fit not applicable Variation Frequency Submission N.D. Genotype Summary N.D. Genotype Submission N.D. Haplotype N.D.   Fasta sequence   (Legend) >gnl|dbSNP|ss783727731|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic ACTTCCAGTT TGGCTTCTGT CCTCA Y AGTCTCTCTC CATGTGGCAA ACAAG   Submitted Frequency for ss783727731 There is no frequency submission for ss783727731.   dbSNP summary of Genotypes for ss783727731 No sufficient data to compute Hardy-weinberg probability for ss783727731.   Submitted individual genotype for ss783727731 There is no individual genotype data for ss783727731.

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