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: ss778717296           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni25Exome-8v1_A_rs9701779-131_B_R_1867868368
RefSNP(rs#)rs9701779
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 AlleleA/G
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|ss778717296|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 CTTTCACTTC TGAGTCCCAG AGGTT
 R
 CCCAAGGCAC CCCTCTGACA TCCGG

  Submitted Frequency for ss778717296 back to top
There is no frequency submission for ss778717296.


  dbSNP summary of Genotypes for ss778717296 back to top
No sufficient data to compute Hardy-weinberg probability for ss778717296.


  Submitted individual genotype for ss778717296 back to top
There is no individual genotype data for ss778717296.