Submitter Handle ILLUMINA Submitter SNP ID OmniExpressExome-8v1-1_B_exm1225955-0_T_F_1921754663 RefSNP(rs#) rs5738 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 G/A Ancestral Allele N.D. Allele Origin G:Germline A: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|ss1752186847|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic CAAGGCTTCA AATGTCATGC ACATC R AGTCCAAGCA AGTGGTGGGA TTCCA   Submitted Frequency for ss1752186847 There is no frequency submission for ss1752186847.   dbSNP summary of Genotypes for ss1752186847 No sufficient data to compute Hardy-weinberg probability for ss1752186847.   Submitted individual genotype for ss1752186847 There is no individual genotype data for ss1752186847.

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