Submitter Handle ILLUMINA Submitter SNP ID HumanOmni1-Quad_v1-0_C_rs6122-131_B_F_1863453958 RefSNP(rs#) rs6122 Submitted Batch ID HumanOmni1-Quad_v1-0_C Submitted Date Jan 30, 2012 Publication Cited N.D. First entry to dbSNP Jan 30 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-CHIP Ascertainment Samplesize 2 Population N.D. Allele Observed Allele G/A 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|ss482229689|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic TTGATAGTTT CCATAAATGC TTACC R TTTCCGGGTC ATTTTCAAAG ACCTC   Submitted Frequency for ss482229689 There is no frequency submission for ss482229689.   dbSNP summary of Genotypes for ss482229689 No sufficient data to compute Hardy-weinberg probability for ss482229689.   Submitted individual genotype for ss482229689 There is no individual genotype data for ss482229689.

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