Submitter Handle PJP Submitter SNP ID DIP_487022_chr20_41633119 RefSNP(rs#) rs66990609 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 GTGT/- 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|ss295049318|allelePos=52|len=103|taxid=9606|alleles='GTGT/-'|mol=Genomic TTTTCTGCAG GGATCTGAAA CCAGAGAACA TTCTCTTGGA CTGCCAGGTT G N GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTATGTGG TTGCACAGGT A   Submitted Frequency for ss295049318 There is no frequency submission for ss295049318.   dbSNP summary of Genotypes for ss295049318 No sufficient data to compute Hardy-weinberg probability for ss295049318.   Submitted individual genotype for ss295049318 There is no individual genotype data for ss295049318.

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