Submitter Handle ILLUMINA Submitter SNP ID HumanExome-12v1-1_B_exm1649-0_T_F_1921527129 RefSNP(rs#) rs74475385 Submitted Batch ID HumanExome-12v1-1 Submitted Date Oct 16, 2015 Publication Cited N.D. First entry to dbSNP Oct 16 2015 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 242901 Population N.D. Allele Observed Allele A/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|ss1917721008|allelePos=26|len=51|taxid=9606|alleles='A/C'|mol=Genomic AAGGACTGGG TCTTCACCAC CCTCA M GGTGCGTCCA CTGTGCCCTC CAGTC   Submitted Frequency for ss1917721008 There is no frequency submission for ss1917721008.   dbSNP summary of Genotypes for ss1917721008 No sufficient data to compute Hardy-weinberg probability for ss1917721008.   Submitted individual genotype for ss1917721008 There is no individual genotype data for ss1917721008.

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