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Submitted SNP(ss) Details: ss479153661           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpress-12v1_C_rs10000119-131_T_R_1856971927
RefSNP(rs#)rs10000119
Submitted Batch IDHumanOmniExpress-12v1_C
Submitted DateJan 30, 2012
Publication CitedN.D.
First entry to dbSNPJan 30 2012 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize2
PopulationN.D.
Allele
Observed AlleleC/T
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|ss479153661|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 AAGTGGTACT TGGTCAAATA CATGT
 Y
 GGTGATGGCG CTCACATTTT GGTTC

  Submitted Frequency for ss479153661 back to top
There is no frequency submission for ss479153661.


  dbSNP summary of Genotypes for ss479153661 back to top
No sufficient data to compute Hardy-weinberg probability for ss479153661.


  Submitted individual genotype for ss479153661 back to top
There is no individual genotype data for ss479153661.

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