Submitter Handle ILLUMINA Submitter SNP ID HumanOmni1-Quad_v1-0_C_rs942379-131_B_R_1865769957 RefSNP(rs#) rs942379 Submitted Batch ID HumanOmni1-Quad_v1-0_C 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 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|ss482888030|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic ATTGTACCTG ACTAAGAAGA AATCC R CTGACAGTGG GTACAATGAC AGGTG   Submitted Frequency for ss482888030 There is no frequency submission for ss482888030.   dbSNP summary of Genotypes for ss482888030 No sufficient data to compute Hardy-weinberg probability for ss482888030.   Submitted individual genotype for ss482888030 There is no individual genotype data for ss482888030.

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