Submitter Handle ILLUMINA Submitter SNP ID HumanOmni25Exome-8v1_A_rs41115-131_T_R_1865541603 RefSNP(rs#) rs41115 Submitted Batch ID HumanOmni25Exome-8v1_A Submitted Date May 30, 2013 Publication Cited N.D. First entry to dbSNP May 30 2013 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 G/A Ancestral Allele N.D. Allele Origin T: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|ss778530117|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic CTGATACTTT ATTACATTTT GCCAC R GAAAGTACTC CAGATGGATT TTCTT   Submitted Frequency for ss778530117 There is no frequency submission for ss778530117.   dbSNP summary of Genotypes for ss778530117 No sufficient data to compute Hardy-weinberg probability for ss778530117.   Submitted individual genotype for ss778530117 There is no individual genotype data for ss778530117.

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