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Submitted SNP(ss) Details: ss479397123           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpress-12v1_C_rs10894147-131_B_F_1857174150
RefSNP(rs#)rs10894147
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|ss479397123|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 CCTAAGTCTC TCCCCTATTA TTGCA
 Y
 GAATAGTGTA CCAGCACCAG ACTAG

  Submitted Frequency for ss479397123 back to top
There is no frequency submission for ss479397123.


  dbSNP summary of Genotypes for ss479397123 back to top
No sufficient data to compute Hardy-weinberg probability for ss479397123.


  Submitted individual genotype for ss479397123 back to top
There is no individual genotype data for ss479397123.

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