Submitter Handle ILLUMINA Submitter SNP ID HumanOmni2.5-4v1_D_rs2295766-131_B_F_1857196910 RefSNP(rs#) rs2295766 Submitted Batch ID HumanOmni2.5-4v1_D 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 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|ss485056055|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic AGCCTTGTCA ATGGATCCAC TGAGC Y CGGAGAGAGC AACTCCGCAA TTTTA   Submitted Frequency for ss485056055 There is no frequency submission for ss485056055.   dbSNP summary of Genotypes for ss485056055 No sufficient data to compute Hardy-weinberg probability for ss485056055.   Submitted individual genotype for ss485056055 There is no individual genotype data for ss485056055.

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