Submitter Handle ILLUMINA Submitter SNP ID OmniExpressExome-8v1-1_B_rs5110-131_B_F_1893184362 RefSNP(rs#) rs5110 Submitted Batch ID HumanOmniExpressExome8v1-1_B Submitted Date May 27, 2015 Publication Cited N.D. First entry to dbSNP May 27 2015 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-CUSTOMERIZED-CHIP Ascertainment Samplesize 2 Population N.D. Allele Observed Allele C/A Ancestral Allele N.D. Allele Origin G:Germline T:Germline 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|ss1751996781|allelePos=26|len=51|taxid=9606|alleles='C/A'|mol=Genomic GCACCTGCTC CTGCTGCTGC TCCTG M TGCTGTTCCT GCTGTTGCTC CAGCT   Submitted Frequency for ss1751996781 There is no frequency submission for ss1751996781.   dbSNP summary of Genotypes for ss1751996781 No sufficient data to compute Hardy-weinberg probability for ss1751996781.   Submitted individual genotype for ss1751996781 There is no individual genotype data for ss1751996781.

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