Submitter Handle ILLUMINA Submitter SNP ID HumanOmni25Exome-8v1_A_kgp22782406-0_B_R_1860537647 RefSNP(rs#) rs5916687 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 G/A 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|ss780063799|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic TAAATGAAAA TTTGTGATAG CTATT R GAAAAGAACA GATAAAATTA GAGCA   Submitted Frequency for ss780063799 There is no frequency submission for ss780063799.   dbSNP summary of Genotypes for ss780063799 No sufficient data to compute Hardy-weinberg probability for ss780063799.   Submitted individual genotype for ss780063799 There is no individual genotype data for ss780063799.

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