Submitter Handle ILLUMINA Submitter SNP ID Human1M-Duov3_B_200521-0_B_R_1526882038 RefSNP(rs#) rs383711 Submitted Batch ID Human1M-Duov3_B Submitted Date Oct 01, 2009 Publication Cited N.D. First entry to dbSNP Oct 1 2009 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-CUSTOMERIZED-CHIP Ascertainment Samplesize 270 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|ss168870912|allelePos=61|len=121|taxid=9606|alleles='C/T'|mol=Genomic CCTCTCCACA GACACCAACC ACCAGTCCCC TAGAAAATCC CCAAACTTTG GGGATCTCTT Y ATTCAGGCCC CCTTCCCAGG GACCCCACTA CATTCAGTGC TCACCCTCAG GGTCCCCCAA   Submitted Frequency for ss168870912 There is no frequency submission for ss168870912.   dbSNP summary of Genotypes for ss168870912 No sufficient data to compute Hardy-weinberg probability for ss168870912.   Submitted individual genotype for ss168870912 There is no individual genotype data for ss168870912.

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