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Submitted SNP(ss) Details: ss779456953           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni25Exome-8v1_A_kgp15921763-0_B_F_1838546317
RefSNP(rs#)rs3795322
Submitted Batch IDHumanOmni25Exome-8v1_A
Submitted DateMay 30, 2013
Publication CitedN.D.
First entry to dbSNPMay 30 2013 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|ss779456953|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 CACCTATCAG CTCCCAGACG GCTCC
 Y
 GCGTGGAGCT GACCCCCATG CAGCG

  Submitted Frequency for ss779456953 back to top
There is no frequency submission for ss779456953.


  dbSNP summary of Genotypes for ss779456953 back to top
No sufficient data to compute Hardy-weinberg probability for ss779456953.


  Submitted individual genotype for ss779456953 back to top
There is no individual genotype data for ss779456953.