Submitter Handle ILLUMINA Submitter SNP ID HumanOmni25Exome-8v1_A_kgp7903468-0_B_F_1817230694 RefSNP(rs#) rs138931 Submitted Batch ID HumanOmni25Exome-8v1_A Submitted Date May 30, 2013 Publication Cited N.D. First entry to dbSNP May 30 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 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|ss780485734|allelePos=26|len=51|taxid=9606|alleles='C/G'|mol=Genomic AGTTACGAGG CCTGCTCAGA ACAGC S TCTCAAGAGG GGGTCTGCTG CCCCT   Submitted Frequency for ss780485734 There is no frequency submission for ss780485734.   dbSNP summary of Genotypes for ss780485734 No sufficient data to compute Hardy-weinberg probability for ss780485734.   Submitted individual genotype for ss780485734 There is no individual genotype data for ss780485734.

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