Submitter Handle ILLUMINA Submitter SNP ID HumanOmni2.5-8v1_A_rs6647613-131_B_R_1865737271 RefSNP(rs#) rs6647613 Submitted Batch ID HumanOmni2.5-8v1_A Submitted Date Sep 18, 2013 Publication Cited N.D. First entry to dbSNP Sep 18 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/C 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|ss833796951|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic CTTACAATCA TACGAAAAAA AAATA S CTTTGTATCT CTTAGTGGGA AAATT   Submitted Frequency for ss833796951 There is no frequency submission for ss833796951.   dbSNP summary of Genotypes for ss833796951 No sufficient data to compute Hardy-weinberg probability for ss833796951.   Submitted individual genotype for ss833796951 There is no individual genotype data for ss833796951.

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