Submitter Handle MCHAISSO Submitter SNP ID HG0073310828 RefSNP(rs#) rs753003396 Submitted Batch ID HG00733 Submitted Date Sep 15, 2017 Publication Cited [1] Multi-platform discovery of haplotype-resolved structural variation in human genomes First entry to dbSNP Sep 15 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 UNIFIEDCALLSET Ascertainment Samplesize 46 Population CHS-PUR-YRI Allele Observed Allele -/AG Ancestral Allele N.D. Allele Origin N/A SNP Class DIV 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|ss3064396772|allelePos=26|len=51|taxid=9606|alleles='-/AG'|mol=Genomic TGGCTCTCCT TATTTCTCCT CCAGC N AGAGAGAGAG AGAGAGAGAG AGAGA   Submitted Frequency for ss3064396772 There is no frequency submission for ss3064396772.   dbSNP summary of Genotypes for ss3064396772 No sufficient data to compute Hardy-weinberg probability for ss3064396772.   Submitted individual genotype for ss3064396772 There is no individual genotype data for ss3064396772.

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