Submitter Handle ILLUMINA Submitter SNP ID HumanOmniExpress-12v1_C_rs699-131_B_F_1862787252 RefSNP(rs#) rs699 Submitted Batch ID HumanOmniExpress-12v1_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 A/G Ancestral Allele N.D. Allele Origin T: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|ss481451642|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic CAGGGTGCTG TCCACACTGG CTCCC R TCAGGGAGCA GCCAGTCTTC CATCC   Submitted Frequency for ss481451642 There is no frequency submission for ss481451642.   dbSNP summary of Genotypes for ss481451642 No sufficient data to compute Hardy-weinberg probability for ss481451642.   Submitted individual genotype for ss481451642 There is no individual genotype data for ss481451642.

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