Submitter Handle ILLUMINA Submitter SNP ID HumanOmniExpress-12v1_J_rs6681049-131_T_R_1858018399 RefSNP(rs#) clustering in process Submitted Batch ID HumanOmniExpress-12v1_J 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 730525 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|ss3633571437|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic AAGAACCTTT AGGACTGAGC ATGTC Y TTCTGTTTGC TTTAAGCTTT TAAGA   Submitted Frequency for ss3633571437 There is no frequency submission for ss3633571437.   dbSNP summary of Genotypes for ss3633571437 No sufficient data to compute Hardy-weinberg probability for ss3633571437.   Submitted individual genotype for ss3633571437 There is no individual genotype data for ss3633571437.

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