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Submitted SNP(ss) Details: ss485236412           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni2.5-4v1_D_rs4018608-131_T_F_1857530819
RefSNP(rs#)rs4018608
Submitted Batch IDHumanOmni2.5-4v1_D
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 AlleleT/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|ss485236412|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 ACTCTGGAGA CTCCAAGGCA CTCAC
 Y
 GGGCAGAGCA GCTGTCTTCC TGGTA

  Submitted Frequency for ss485236412 back to top
There is no frequency submission for ss485236412.


  dbSNP summary of Genotypes for ss485236412 back to top
No sufficient data to compute Hardy-weinberg probability for ss485236412.


  Submitted individual genotype for ss485236412 back to top
There is no individual genotype data for ss485236412.