Submitter Handle ILLUMINA Submitter SNP ID HumanOmni25Exome-8v1_A_rs17448457-131_T_F_1865481836 RefSNP(rs#) rs17448457 Submitted Batch ID HumanOmni25Exome-8v1_A Submitted Date May 30, 2013 Publication Cited N.D. First entry to dbSNP May 30 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 T/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|ss778342331|allelePos=26|len=51|taxid=9606|alleles='T/A'|mol=Genomic GGGTACTTAG GTCATACATG GGAAT W TGTGGGTAAT GAAGATTCCT GGGAC   Submitted Frequency for ss778342331 There is no frequency submission for ss778342331.   dbSNP summary of Genotypes for ss778342331 No sufficient data to compute Hardy-weinberg probability for ss778342331.   Submitted individual genotype for ss778342331 There is no individual genotype data for ss778342331.

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