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Submitted SNP(ss) Details: ss480839458           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpress-12v1_C_rs3766191-131_T_F_1857482964
RefSNP(rs#)rs3766191
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|ss480839458|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 GCCAGGCATG GGGGTCCAGC GGATC
 Y
 GAGCGGGGCC ACAGAGCTCT GGAGG

  Submitted Frequency for ss480839458 back to top
There is no frequency submission for ss480839458.


  dbSNP summary of Genotypes for ss480839458 back to top
No sufficient data to compute Hardy-weinberg probability for ss480839458.


  Submitted individual genotype for ss480839458 back to top
There is no individual genotype data for ss480839458.