Submitter Handle ILLUMINA Submitter SNP ID HumanOmni1-Quad_v1-0_B_rs506128-126_T_F_1502227340 RefSNP(rs#) rs506128 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 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|ss160737771|allelePos=51|len=101|taxid=9606|alleles='A/G'|mol=Genomic AGAGAGAGAG AAACATGTAT GGCCGATAAA CACAAGAGAA GATTTTCAAC R TGTTTAATGA TCAGAGAAAC ACATTATAAT CTCTAAAATT TGTTTTTACC   Submitted Frequency for ss160737771 There is no frequency submission for ss160737771.   dbSNP summary of Genotypes for ss160737771 No sufficient data to compute Hardy-weinberg probability for ss160737771.   Submitted individual genotype for ss160737771 There is no individual genotype data for ss160737771.

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