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Submitted SNP(ss) Details: ss783046902           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni2.5-4v1_H_rs3748932-131_B_R_1857475111
RefSNP(rs#)rs3748932
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|ss783046902|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 TACGTCACCC AGTGAATGAT GTGGT
 Y
 CCCAAACTGA AGGTCTAGCC ATCTG

  Submitted Frequency for ss783046902 back to top
There is no frequency submission for ss783046902.


  dbSNP summary of Genotypes for ss783046902 back to top
No sufficient data to compute Hardy-weinberg probability for ss783046902.


  Submitted individual genotype for ss783046902 back to top
There is no individual genotype data for ss783046902.