Submitter Handle ILLUMINA Submitter SNP ID HumanCNV370-Quadv3_C_rs2295767-128_T_R_1501728830 RefSNP(rs#) rs2295767 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 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|ss171174451|allelePos=61|len=121|taxid=9606|alleles='G/A'|mol=Genomic TTCCTTGGTG TACCCGTGAT GCCTTTCAGT GTTTGGTATA CCTCTTCTGG ATCAATCCAC R TTTTAATTTT GAGGAGGGGG TTAGTGTGTT AATGTTAATA TAGTTTTTCC TTTCACAAGT   Submitted Frequency for ss171174451 There is no frequency submission for ss171174451.   dbSNP summary of Genotypes for ss171174451 No sufficient data to compute Hardy-weinberg probability for ss171174451.   Submitted individual genotype for ss171174451 There is no individual genotype data for ss171174451.

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