Submitter Handle ILLUMINA Submitter SNP ID HumanOmni5Exome-4v1_A_rs17120680-131_B_F_1894849537 RefSNP(rs#) clustering in process Submitted Batch ID HumanOmni5Exome-4v1_A_build37 Submitted Date Nov 28, 2017 Publication Cited N.D. First entry to dbSNP Nov 28 2017 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 242901 Population N.D. Allele Observed Allele T/C 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 Homozygote Detected PCR Confirmed In Expressed Sequence Variation Frequency Submission N.D. Genotype Summary N.D. Genotype Submission N.D. Haplotype N.D.   Fasta sequence   (Legend) >gnl|dbSNP|ss3626165260|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic GAGAGCCAAT TAACGTAAGG TGTAT Y TGGATTCTGT TTGATATAGC ATGAG   Submitted Frequency for ss3626165260 There is no frequency submission for ss3626165260.   dbSNP summary of Genotypes for ss3626165260 No sufficient data to compute Hardy-weinberg probability for ss3626165260.   Submitted individual genotype for ss3626165260 There is no individual genotype data for ss3626165260.

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