Submitter Handle ILLUMINA Submitter SNP ID HumanOmniExpressExome-8v1_A_exm-rs9388489-131_B_R_1990486095 RefSNP(rs#) rs9388489 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 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|ss783360981|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic GAAGGTGATA GTTAAATGCC TTGTT R GATTTTTTAG CCAGTGTGAG TCTGT   Submitted Frequency for ss783360981 There is no frequency submission for ss783360981.   dbSNP summary of Genotypes for ss783360981 No sufficient data to compute Hardy-weinberg probability for ss783360981.   Submitted individual genotype for ss783360981 There is no individual genotype data for ss783360981.

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