Submitter Handle ILLUMINA Submitter SNP ID HumanOmni2.5-4v1_B_SNP1-20479055-0_T_R_1633468067 RefSNP(rs#) rs3107 Submitted Batch ID HumanOmni2.5-4v1_B 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 G/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|ss482207076|allelePos=26|len=51|taxid=9606|alleles='G/T'|mol=Genomic AACTTGGTTT TTTGTTGTTG TTGTT K TTTTAATTAT AAGAATAATA TGTGC   Submitted Frequency for ss482207076 There is no frequency submission for ss482207076.   dbSNP summary of Genotypes for ss482207076 No sufficient data to compute Hardy-weinberg probability for ss482207076.   Submitted individual genotype for ss482207076 There is no individual genotype data for ss482207076.

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