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: ss159846007           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni1-Quad_v1-0_B_500556-0_T_F_1526882059
RefSNP(rs#)rs3816511
Submitted Batch IDHumanOmni1-Quad_v1-0_B
Submitted DateAug 04, 2009
Publication CitedN.D.
First entry to dbSNPAug 4 2009 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CUSTOMERIZED-CHIP
Ascertainment Samplesize270
PopulationN.D.
Allele
Observed AlleleG/A
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|ss159846007|allelePos=61|len=121|taxid=9606|alleles='G/A'|mol=Genomic
 AGGGGAGAGG GGCCGGCTGC CTGCTGGGTC CTGCAGGCCG CATTGTAAGC TACCATGGCC
 R
 CTCTGACCTG GGAGCCCTGG AGTGGGCCTG GCTGACGGCA GCCTGTCCTG AGCCTGCCCT

  Submitted Frequency for ss159846007 back to top
There is no frequency submission for ss159846007.


  dbSNP summary of Genotypes for ss159846007 back to top
No sufficient data to compute Hardy-weinberg probability for ss159846007.


  Submitted individual genotype for ss159846007 back to top
There is no individual genotype data for ss159846007.