Submitter Handle PJP Submitter SNP ID DIP_54340_chr1_188392277 RefSNP(rs#) rs34512031 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|ss294616636|allelePos=52|len=103|taxid=9606|alleles='T/-'|mol=Genomic TTACATTCTA CCATATTCTA CCCTCCTAGA ATCCAGTACA TATTTTTTTT T N GTTTTCCTGA TGTCATTTCA TATTATTCTT TTAAAATGGA AAAAAAGAGA G   Submitted Frequency for ss294616636 There is no frequency submission for ss294616636.   dbSNP summary of Genotypes for ss294616636 No sufficient data to compute Hardy-weinberg probability for ss294616636.   Submitted individual genotype for ss294616636 There is no individual genotype data for ss294616636.

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