Submitter Handle ILLUMINA Submitter SNP ID HumanCoreExome-12v1-0_C_exm2263307-0_B_F_1978044876 RefSNP(rs#) rs201801609 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 C/T 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|ss1945966267|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic GCCACTTTCC ACACAGACAT CATAA Y AAAAAATTTC CACCAAACCC CCCCT   Submitted Frequency for ss1945966267 There is no frequency submission for ss1945966267.   dbSNP summary of Genotypes for ss1945966267 No sufficient data to compute Hardy-weinberg probability for ss1945966267.   Submitted individual genotype for ss1945966267 There is no individual genotype data for ss1945966267.

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