Submitter Handle ILLUMINA Submitter SNP ID HumanOmniExpress-12v1_C_rs1000002-131_T_F_1856971897 RefSNP(rs#) rs1000002 Submitted Batch ID HumanOmniExpress-12v1_C Submitted Date Jan 30, 2012 Publication Cited N.D. First entry to dbSNP Jan 30 2012 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|ss479153622|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic CAAGTACTAG CTCTGATGGT TCTCA Y TTGGACAGCA GCCAGCTTAG TCCTC   Submitted Frequency for ss479153622 There is no frequency submission for ss479153622.   dbSNP summary of Genotypes for ss479153622 No sufficient data to compute Hardy-weinberg probability for ss479153622.   Submitted individual genotype for ss479153622 There is no individual genotype data for ss479153622.

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