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Submitted SNP(ss) Details: ss481950922           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni2.5-4v1_B_rs9614-128_T_F_1765577633
RefSNP(rs#)rs9614
Submitted Batch IDHumanOmni2.5-4v1_B
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 AlleleT/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|ss481950922|allelePos=26|len=51|taxid=9606|alleles='T/G'|mol=Genomic
 GTTACGCAGA AGGTTGCGGC GCCGC
 K
 TGCTCAGGAA GTAGAACTGC TGCCA

  Submitted Frequency for ss481950922 back to top
There is no frequency submission for ss481950922.


  dbSNP summary of Genotypes for ss481950922 back to top
No sufficient data to compute Hardy-weinberg probability for ss481950922.


  Submitted individual genotype for ss481950922 back to top
There is no individual genotype data for ss481950922.

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