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Submitted SNP(ss) Details: ss485351569           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni2.5-4v1_D_rs4952-131_B_F_1857733690
RefSNP(rs#)rs4952
Submitted Batch IDHumanOmni2.5-4v1_D
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|ss485351569|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 ATAACGGAGA ATGGGAAATA CTGAA
 Y
 GCAAAGGGGA TGAAGGGGAA CAGAA

  Submitted Frequency for ss485351569 back to top
There is no frequency submission for ss485351569.


  dbSNP summary of Genotypes for ss485351569 back to top
No sufficient data to compute Hardy-weinberg probability for ss485351569.


  Submitted individual genotype for ss485351569 back to top
There is no individual genotype data for ss485351569.