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Submitted SNP(ss) Details: ss484376862           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni2.5-4v1_D_MitoA11252G-0_B_R_1852011184
RefSNP(rs#)rs869096886
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 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|ss484376862|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 GCTCCCTTCC CCTACTCATC GCACT
 R
 ATTTACACTC ACAACACCCT AGGCT

  Submitted Frequency for ss484376862 back to top
There is no frequency submission for ss484376862.


  dbSNP summary of Genotypes for ss484376862 back to top
No sufficient data to compute Hardy-weinberg probability for ss484376862.


  Submitted individual genotype for ss484376862 back to top
There is no individual genotype data for ss484376862.