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Submitted SNP(ss) Details: ss537610668           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni5-4v1_B_rs9550383-131_B_F_1866906152
RefSNP(rs#)rs9550383
Submitted Batch IDHumanOmni5-4v1_B
Submitted DateJun 22, 2012
Publication CitedN.D.
First entry to dbSNPJun 22 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|ss537610668|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 TGCATTCCTT TCTGATGGCT TATCA
 Y
 ATTGCACTCT GGGTTAAATG CCATA

  Submitted Frequency for ss537610668 back to top
There is no frequency submission for ss537610668.


  dbSNP summary of Genotypes for ss537610668 back to top
No sufficient data to compute Hardy-weinberg probability for ss537610668.


  Submitted individual genotype for ss537610668 back to top
There is no individual genotype data for ss537610668.

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