Submitter Handle PJP Submitter SNP ID DIP_174719_chr12_12749331 RefSNP(rs#) rs386375641 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 -/TT 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|ss294737015|allelePos=52|len=103|taxid=9606|alleles='-/TT'|mol=Genomic GAAAGGCTTT TTGTCAAGAA TAAATAGAAA TGCATCTTTT TTTTTTTTTT T N TGAGACGGAG TCTTGCTCTC TAACCCAGGC TGGAGTGCAG TGGTGCGATC T   Submitted Frequency for ss294737015 There is no frequency submission for ss294737015.   dbSNP summary of Genotypes for ss294737015 No sufficient data to compute Hardy-weinberg probability for ss294737015.   Submitted individual genotype for ss294737015 There is no individual genotype data for ss294737015.

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