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Submitted SNP(ss) Details: ss161003807           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni1-Quad_v1-0_B_rs9614-128_T_F_1501893478
RefSNP(rs#)rs9614
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 AlleleA/C
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|ss161003807|allelePos=61|len=121|taxid=9606|alleles='A/C'|mol=Genomic
 TGCCCGAGGG CGGCGTGGAG GAGGAGCGCG ACCACTGGCA GCAGTTCTAC TTCCTGAGCA
 M
 GCGGCGCCGC AACCTTCTGC GTAACCCGTG TGGGGAAGGT GAGAGGCCCT CGCTGGGCGA

  Submitted Frequency for ss161003807 back to top
There is no frequency submission for ss161003807.


  dbSNP summary of Genotypes for ss161003807 back to top
No sufficient data to compute Hardy-weinberg probability for ss161003807.


  Submitted individual genotype for ss161003807 back to top
There is no individual genotype data for ss161003807.