NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss1751884980           
Submitter
HandleILLUMINA
Submitter SNP IDOmniExpressExome-8v1-1_B_exm24180-0_B_F_1921542691
RefSNP(rs#)rs3795322
Submitted Batch IDHumanOmniExpressExome8v1-1_B
Submitted DateMay 27, 2015
Publication CitedN.D.
First entry to dbSNPMay 27 2015 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CUSTOMERIZED-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|ss1751884980|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 CACCTATCAG CTCCCAGACG GCTCC
 Y
 GCGTGGAGCT GACCCCCATG CAGCG

  Submitted Frequency for ss1751884980 back to top
There is no frequency submission for ss1751884980.


  dbSNP summary of Genotypes for ss1751884980 back to top
No sufficient data to compute Hardy-weinberg probability for ss1751884980.


  Submitted individual genotype for ss1751884980 back to top
There is no individual genotype data for ss1751884980.