Submitter Handle ILLUMINA Submitter SNP ID HumanCNV370-Quadv3_C_cnvi0000051-126_B_F_1514230417 RefSNP(rs#) rs113340822 Submitted Batch ID HumanCNV370-Quadv3_C 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 T/C 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|ss168876747|allelePos=54|len=111|taxid=9606|alleles='T/C'|mol=Genomic CGTCGGTCCT CCCTCCTCCG TGGCCACTCT TCAGATGGAT TCACGTCGGT CCT Y CCTCCTCCGT GGCCACTCTT CAGATGGCTT CATGTCGGTC CTCCCTCCTC CGTGGCC   Submitted Frequency for ss168876747 There is no frequency submission for ss168876747.   dbSNP summary of Genotypes for ss168876747 No sufficient data to compute Hardy-weinberg probability for ss168876747.   Submitted individual genotype for ss168876747 There is no individual genotype data for ss168876747.

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