Submitter Handle PJP Submitter SNP ID DIP_306964_chr15_76702437 RefSNP(rs#) rs34573245 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|ss294869260|allelePos=52|len=103|taxid=9606|alleles='T/-'|mol=Genomic CAGAAAACAG TTTGACAGTT TCTTTCTCTT TCTTTTGTTC TTTTTTTTTT T N GACAGAGTCT CGCTCTGTCA CCCAGGCTGG AGTGCAGTGG CACGATCTCG G   Submitted Frequency for ss294869260 There is no frequency submission for ss294869260.   dbSNP summary of Genotypes for ss294869260 No sufficient data to compute Hardy-weinberg probability for ss294869260.   Submitted individual genotype for ss294869260 There is no individual genotype data for ss294869260.

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