Submitter Handle ILLUMINA Submitter SNP ID HumanOmni1-Quad_v1-0_C_rs3737728-131_T_R_1865417923 RefSNP(rs#) rs3737728 Submitted Batch ID HumanOmni1-Quad_v1-0_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 A/G 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|ss481748289|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic CCCCTGCAAA CAGACACCGC TGAGC R GACGGGCAGG ACGGTGGCCC TGGCT   Submitted Frequency for ss481748289 There is no frequency submission for ss481748289.   dbSNP summary of Genotypes for ss481748289 No sufficient data to compute Hardy-weinberg probability for ss481748289.   Submitted individual genotype for ss481748289 There is no individual genotype data for ss481748289.

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