Submitter Handle PJP Submitter SNP ID DIP_157474_chr11_102002967 RefSNP(rs#) rs10617728 Submitted Batch ID NSMB2011_INDEL Submitted Date Jan 21, 2011 Publication Cited [1] Impact of chromatin structure on sequence variability in the human genome First entry to dbSNP Jan 21 2011 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 TRACESALIGNMENT Ascertainment Samplesize N.D. Population N.D. Allele Observed Allele GAAT/- Ancestral Allele N.D. Allele Origin N/A SNP Class DIV 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|ss294719770|allelePos=52|len=103|taxid=9606|alleles='GAAT/-'|mol=Genomic TGAAGACTGT ATTCTAAAAA ATGTTACTTA ATCAAGTTTG TTAAAAAAAA A N GAATGAATGT ACAAACATAT ACTAATCATT GCTTTTTGGT TTCAGGAAAG G   Submitted Frequency for ss294719770 There is no frequency submission for ss294719770.   dbSNP summary of Genotypes for ss294719770 No sufficient data to compute Hardy-weinberg probability for ss294719770.   Submitted individual genotype for ss294719770 There is no individual genotype data for ss294719770.

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