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Submitted SNP(ss) Details: ss2137543832           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpressExome-8v1-2_A_rs4477212-131_B_R_1894896677
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmniExpressExome-8v1-2_A
Submitted DateDec 07, 2017
Publication CitedN.D.
First entry to dbSNPDec 7 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize964193
PopulationN.D.
Allele
Observed AlleleA/G
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss2137543832|allelePos=1|len=1|taxid=9606|alleles='A/G'|mol=Genomic
 R

  Submitted Frequency for ss2137543832 back to top
There is no frequency submission for ss2137543832.


  dbSNP summary of Genotypes for ss2137543832 back to top
No sufficient data to compute Hardy-weinberg probability for ss2137543832.


  Submitted individual genotype for ss2137543832 back to top
There is no individual genotype data for ss2137543832.

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