Submitter Handle ILLUMINA Submitter SNP ID SoL_HCHS_Custom_15041502_B3_RefStrand_SoL-rs8192284-128_B_R_2131 RefSNP(rs#) rs2228145 Submitted Batch ID SoL_HCHS_Custom_15041502_B3_RefStrand Submitted Date Feb 02, 2017 Publication Cited N.D. First entry to dbSNP Feb 2 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 2536661 Population N.D. Allele Observed Allele A/C Ancestral Allele N.D. Allele Origin A:Germline C:Germline 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|ss2632575971|allelePos=26|len=51|taxid=9606|alleles='A/C'|mol=Genomic AATTTTTTTT TTAACCTAGT GCAAG M TTCTTCTTCA GTACCACTGC CCACA   Submitted Frequency for ss2632575971 There is no frequency submission for ss2632575971.   dbSNP summary of Genotypes for ss2632575971 No sufficient data to compute Hardy-weinberg probability for ss2632575971.   Submitted individual genotype for ss2632575971 There is no individual genotype data for ss2632575971.

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