Submitter Handle ILLUMINA Submitter SNP ID HumanOmni1-Quad_v1-0_B_rs11260542-128_B_R_1514023887 RefSNP(rs#) rs11260542 Submitted Batch ID HumanOmni1-Quad_v1-0_B Submitted Date Aug 04, 2009 Publication Cited N.D. First entry to dbSNP Aug 4 2009 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-CUSTOMERIZED-CHIP Ascertainment Samplesize 270 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|ss159976149|allelePos=61|len=121|taxid=9606|alleles='C/T'|mol=Genomic AGTCTCTGAC GGACGCGATT CTGAATCCAG AAGGAAAGCG TCTCACTCCG AGATGCTGAC Y GACGTGTCCT TTATAGCGGT GGGACTTGGG AAGCCGGTGA CGCCCGGTGT GGAGGACGGT   Submitted Frequency for ss159976149 There is no frequency submission for ss159976149.   dbSNP summary of Genotypes for ss159976149 No sufficient data to compute Hardy-weinberg probability for ss159976149.   Submitted individual genotype for ss159976149 There is no individual genotype data for ss159976149.

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