Submitter Handle ILLUMINA Submitter SNP ID HumanOmni1-Quad_v1-0_B_rs1339856-128_B_F_1545751342 RefSNP(rs#) rs1339856 Submitted Batch ID HumanOmni1-Quad_v1-0_B Submitted Date Aug 04, 2009 Publication Cited N.D. First entry to dbSNP Aug 4 2009 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-CUSTOMERIZED-CHIP Ascertainment Samplesize 270 Population N.D. Allele Observed Allele T/C Ancestral Allele N.D. Allele Origin N/A 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|ss160335477|allelePos=61|len=121|taxid=9606|alleles='T/C'|mol=Genomic ATACATTGCC CCACATACAT TTGACTTCAC TAACTACCTG ATTTATGAAT CTTTTCTAAA Y ATTAATTAAG GCCCAGATTC TGCTTGAACA AGTTAAGTAG TGATGATCTC AGTCTCACTA   Submitted Frequency for ss160335477 There is no frequency submission for ss160335477.   dbSNP summary of Genotypes for ss160335477 No sufficient data to compute Hardy-weinberg probability for ss160335477.   Submitted individual genotype for ss160335477 There is no individual genotype data for ss160335477.

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