Submitter Handle ILLUMINA Submitter SNP ID HumanOmniExpressExome-8v1_A_exm686341-0_T_F_1922954829 RefSNP(rs#) rs328 Submitted Batch ID HumanOmniExpressExome-8v1_A Submitted Date May 31, 2013 Publication Cited N.D. First entry to dbSNP May 31 2013 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 C/G Ancestral Allele N.D. Allele Origin G:Germline C:Germline 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|ss783552875|allelePos=26|len=51|taxid=9606|alleles='C/G'|mol=Genomic CATGACAAGT CTCTGAATAA GAAGT S AGGCTGGTGA GCATTCTGGG CTAAA   Submitted Frequency for ss783552875 There is no frequency submission for ss783552875.   dbSNP summary of Genotypes for ss783552875 No sufficient data to compute Hardy-weinberg probability for ss783552875.   Submitted individual genotype for ss783552875 There is no individual genotype data for ss783552875.

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