Submitter Handle ILLUMINA Submitter SNP ID HumanOmniExpressExome-8v1-2_A_rs2297630-131_B_R_1885569985 RefSNP(rs#) clustering in process Submitted Batch ID HumanOmniExpressExome-8v1-2_A Submitted Date Dec 07, 2017 Publication Cited N.D. First entry to dbSNP Dec 7 2017 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 964193 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 Homozygote Detected PCR Confirmed In Expressed Sequence Variation Frequency Submission N.D. Genotype Summary N.D. Genotype Submission N.D. Haplotype N.D.   Fasta sequence   (Legend) >gnl|dbSNP|ss3634401008|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic CAAAAGTTCG TCTCAGTCTG CATAA R ATTTAACACT GGCCCGTGTA CTGGT   Submitted Frequency for ss3634401008 There is no frequency submission for ss3634401008.   dbSNP summary of Genotypes for ss3634401008 No sufficient data to compute Hardy-weinberg probability for ss3634401008.   Submitted individual genotype for ss3634401008 There is no individual genotype data for ss3634401008.

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