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: ss482888116           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni1-Quad_v1-0_C_rs9424290-131_B_F_1865476553
RefSNP(rs#)rs9424290
Submitted Batch IDHumanOmni1-Quad_v1-0_C
Submitted DateJan 30, 2012
Publication CitedN.D.
First entry to dbSNPJan 30 2012 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|ss482888116|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 CTATAAAGCA AGAAATCCAA CATGA
 Y
 GCCACATGGT TCCGTTTCTA CAAAG

  Submitted Frequency for ss482888116 back to top
There is no frequency submission for ss482888116.


  dbSNP summary of Genotypes for ss482888116 back to top
No sufficient data to compute Hardy-weinberg probability for ss482888116.


  Submitted individual genotype for ss482888116 back to top
There is no individual genotype data for ss482888116.