Submitter Handle ILLUMINA Submitter SNP ID HumanCoreExome-12v1-0_C_exm1479457-0_B_R_1920935351 RefSNP(rs#) rs5126 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 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 Variation Frequency Submission N.D. Genotype Summary N.D. Genotype Submission N.D. Haplotype N.D.   Fasta sequence   (Legend) >gnl|dbSNP|ss1946537680|allelePos=26|len=51|taxid=9606|alleles='A/C'|mol=Genomic CTTTCTCCCC AGGGACTTGT ACAGC M AAAGCACAGC AGCCATGAGC ACTTA   Submitted Frequency for ss1946537680 There is no frequency submission for ss1946537680.   dbSNP summary of Genotypes for ss1946537680 No sufficient data to compute Hardy-weinberg probability for ss1946537680.   Submitted individual genotype for ss1946537680 There is no individual genotype data for ss1946537680.

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