Submitter Handle GENOMED Submitter SNP ID rs1801166 RefSNP(rs#) rs1801166 Submitted Batch ID UDTseq_CL1 Submitted Date Feb 05, 2016 Publication Cited [1] Discovery of variants in breast cancer patients from Chile by Ultra-Deep Targeted Sequencing First entry to dbSNP Feb 5 2016 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 MYSEQ_UDTSEQ_CL1 Ascertainment Samplesize 98 Population N.D. Allele Observed Allele G/C Ancestral Allele N.D. Allele Origin G:Germline C:Germline SNP Class SNV 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|ss1966658504|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic AGAAAAGATT GGAACTAGGT CAGCT S AAGATCCTGT GAGCGAAGTT CCAGC   Submitted Frequency for ss1966658504 There is no frequency submission for ss1966658504.   dbSNP summary of Genotypes for ss1966658504 No sufficient data to compute Hardy-weinberg probability for ss1966658504.   Submitted individual genotype for ss1966658504 There is no individual genotype data for ss1966658504.

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