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Submitted SNP(ss) Details: ss3633598275           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpress-12v1_J_rs1000792-131_B_R_1856974062
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmniExpress-12v1_J
Submitted DateNov 28, 2017
Publication CitedN.D.
First entry to dbSNPNov 28 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize730525
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
Homozygote Detected
PCR Confirmed
In Expressed Sequence
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss3633598275|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 CAGAGGCACC AAAAGACAAA GAAAT
 R
 TACTCAAGAC CTACTCTTAA TACAT

  Submitted Frequency for ss3633598275 back to top
There is no frequency submission for ss3633598275.


  dbSNP summary of Genotypes for ss3633598275 back to top
No sufficient data to compute Hardy-weinberg probability for ss3633598275.


  Submitted individual genotype for ss3633598275 back to top
There is no individual genotype data for ss3633598275.