Submitter Handle LUNTER Submitter SNP ID CEU_8_121482162-121482165 RefSNP(rs#) rs200517890 Submitted Batch ID indel_calls_from_1000_genomes_pilot_1_CEU Submitted Date Nov 21, 2012 Publication Cited [1] The Origin, evolution and functional impact of short insertion-deletion variants identified in 179 human genomes First entry to dbSNP Nov 21 2012 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 ILLUMINA_SHORT_SEQUENCE_DATA Ascertainment Samplesize 358 Population N.D. Allele Observed Allele AAAA/- 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|ss551890031|allelePos=26|len=51|taxid=9606|alleles='AAAA/-'|mol=Genomic TAAATAAATA AATAAATAAA TAAAT N AAAATAGACT GCTAGTTAGA CTAAT   Submitted Frequency for ss551890031 There is no frequency submission for ss551890031.   dbSNP summary of Genotypes for ss551890031 No sufficient data to compute Hardy-weinberg probability for ss551890031.   Submitted individual genotype for ss551890031 There is no individual genotype data for ss551890031.

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