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Submitted SNP(ss) Details: ss479153664           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpress-12v1_C_rs10000124-131_B_R_1853199531
RefSNP(rs#)rs10000124
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/A
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|ss479153664|allelePos=26|len=51|taxid=9606|alleles='C/A'|mol=Genomic
 TTACACTTTC TTCAAACGCT TTCTT
 M
 CCTTACTTCC AGGATGCCAT CAGCT

  Submitted Frequency for ss479153664 back to top
There is no frequency submission for ss479153664.


  dbSNP summary of Genotypes for ss479153664 back to top
No sufficient data to compute Hardy-weinberg probability for ss479153664.


  Submitted individual genotype for ss479153664 back to top
There is no individual genotype data for ss479153664.

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