Submitter Handle ILLUMINA Submitter SNP ID HumanOmniExpress-12v1_H_rs2295766-131_B_F_1857196910 RefSNP(rs#) rs2295766 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 C/T 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|ss832230616|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic AGCCTTGTCA ATGGATCCAC TGAGC Y CGGAGAGAGC AACTCCGCAA TTTTA   Submitted Frequency for ss832230616 There is no frequency submission for ss832230616.   dbSNP summary of Genotypes for ss832230616 No sufficient data to compute Hardy-weinberg probability for ss832230616.   Submitted individual genotype for ss832230616 There is no individual genotype data for ss832230616.

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