Submitter Handle ILLUMINA Submitter SNP ID HumanOmniExpress-12v1_H_rs555001-131_B_R_1857747765 RefSNP(rs#) rs555001 Submitted Batch ID HumanOmniExpress-12v1_H Submitted Date Sep 17, 2013 Publication Cited N.D. First entry to dbSNP Sep 17 2013 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|ss832388798|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic CCATGGCACA CACCACTCTG CTGAC R TAGACGGGGC TTCCCCGCAG AGCAC   Submitted Frequency for ss832388798 There is no frequency submission for ss832388798.   dbSNP summary of Genotypes for ss832388798 No sufficient data to compute Hardy-weinberg probability for ss832388798.   Submitted individual genotype for ss832388798 There is no individual genotype data for ss832388798.

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