Submitter Handle ILLUMINA Submitter SNP ID HumanCoreExome-12v1-0_C_rs506128-131_T_F_1895136256 RefSNP(rs#) rs506128 Submitted Batch ID HumanCoreExome12v10_c Submitted Date Oct 29, 2015 Publication Cited N.D. First entry to dbSNP Oct 29 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-CHIP Ascertainment Samplesize 2 Population N.D. Allele Observed Allele G/A 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 Variation Frequency Submission N.D. Genotype Summary N.D. Genotype Submission N.D. Haplotype N.D.   Fasta sequence   (Legend) >gnl|dbSNP|ss1946025245|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic ATAAACACAA GAGAAGATTT TCAAC R TGTTTAATGA TCAGAGAAAC ACATT   Submitted Frequency for ss1946025245 There is no frequency submission for ss1946025245.   dbSNP summary of Genotypes for ss1946025245 No sufficient data to compute Hardy-weinberg probability for ss1946025245.   Submitted individual genotype for ss1946025245 There is no individual genotype data for ss1946025245.

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