Submitter Handle PJP Submitter SNP ID DIP_607528_chr4_68037523 RefSNP(rs#) rs67881458 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 AC/- 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|ss295169824|allelePos=52|len=103|taxid=9606|alleles='AC/-'|mol=Genomic AAATATTTTT TATATATATA AAATATTCCT GTTATACATA CACACACACA C N ACACACACAC ATACACACAT ATAAAACAGA CCAATGTTGC AGAGGTGTAT G   Submitted Frequency for ss295169824 There is no frequency submission for ss295169824.   dbSNP summary of Genotypes for ss295169824 No sufficient data to compute Hardy-weinberg probability for ss295169824.   Submitted individual genotype for ss295169824 There is no individual genotype data for ss295169824.

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