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Submitted SNP(ss) Details: ss782670826           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni2.5-4v1_H_rs1050114-128_B_R_1768760782
RefSNP(rs#)rs1050114
Submitted Batch IDHumanOmni2.5-4v1_H
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|ss782670826|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 AAGGAAGCAG GACTGTGAGC GCGGG
 Y
 AGTCGGGGGA AGATAGGAAC CAACG

  Submitted Frequency for ss782670826 back to top
There is no frequency submission for ss782670826.


  dbSNP summary of Genotypes for ss782670826 back to top
No sufficient data to compute Hardy-weinberg probability for ss782670826.


  Submitted individual genotype for ss782670826 back to top
There is no individual genotype data for ss782670826.