Submitter Handle ILLUMINA Submitter SNP ID HumanOmni2.5-4v1_B_SNP1-6447236-0_B_F_1625946461 RefSNP(rs#) rs35137293 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 T/C 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|ss482381078|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic TGTGGCGGTG CAGGGCCCCG CAGTC Y AGGCATGGTT GGCAGTAGAA GGGTG   Submitted Frequency for ss482381078 There is no frequency submission for ss482381078.   dbSNP summary of Genotypes for ss482381078 No sufficient data to compute Hardy-weinberg probability for ss482381078.   Submitted individual genotype for ss482381078 There is no individual genotype data for ss482381078.

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