Submitter Handle ILLUMINA Submitter SNP ID HumanOmni2.5-4v1_H_rs1000792-131_B_R_1856974062 RefSNP(rs#) rs1000792 Submitted Batch ID HumanOmni2.5-4v1_H 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 A/G 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|ss782635529|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic CAGAGGCACC AAAAGACAAA GAAAT R TACTCAAGAC CTACTCTTAA TACAT   Submitted Frequency for ss782635529 There is no frequency submission for ss782635529.   dbSNP summary of Genotypes for ss782635529 No sufficient data to compute Hardy-weinberg probability for ss782635529.   Submitted individual genotype for ss782635529 There is no individual genotype data for ss782635529.

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