Submitter Handle PJP Submitter SNP ID DIP_879851_chr9_132964957 RefSNP(rs#) rs57216561 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 T/- 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|ss295442147|allelePos=52|len=103|taxid=9606|alleles='T/-'|mol=Genomic CTTCCAGAGG GGCAGGGTAG CTCAGCCTTA GCTTTTTTTT TTTTTTTTTT T N AGACAGAGTC TCTGTCACCC AGGCTGGAGT GCAGTGGCGT GATCTCAGTT C   Submitted Frequency for ss295442147 There is no frequency submission for ss295442147.   dbSNP summary of Genotypes for ss295442147 No sufficient data to compute Hardy-weinberg probability for ss295442147.   Submitted individual genotype for ss295442147 There is no individual genotype data for ss295442147.

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