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Submitted SNP(ss) Details: ss831921488           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpress-12v1_H_rs1050114-128_B_R_1768760782
RefSNP(rs#)rs1050114
Submitted Batch IDHumanOmniExpress-12v1_H
Submitted DateSep 17, 2013
Publication CitedN.D.
First entry to dbSNPSep 17 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|ss831921488|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 AAGGAAGCAG GACTGTGAGC GCGGG
 Y
 AGTCGGGGGA AGATAGGAAC CAACG

  Submitted Frequency for ss831921488 back to top
There is no frequency submission for ss831921488.


  dbSNP summary of Genotypes for ss831921488 back to top
No sufficient data to compute Hardy-weinberg probability for ss831921488.


  Submitted individual genotype for ss831921488 back to top
There is no individual genotype data for ss831921488.