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Submitted SNP(ss) Details: ss3633572125           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpress-12v1_J_rs16823940-131_T_R_1857643096
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 AlleleC/T
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|ss3633572125|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 AGCCTCAGCT TCTGAATGTC CCAGA
 Y
 CCAGACGGCA TTGGGAATGT TGTCT

  Submitted Frequency for ss3633572125 back to top
There is no frequency submission for ss3633572125.


  dbSNP summary of Genotypes for ss3633572125 back to top
No sufficient data to compute Hardy-weinberg probability for ss3633572125.


  Submitted individual genotype for ss3633572125 back to top
There is no individual genotype data for ss3633572125.