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Submitted SNP(ss) Details: ss3626006462           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni5Exome-4v1_A_rs9701779-131_B_R_1893927720
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmni5Exome-4v1_A_build37
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 Samplesize242901
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|ss3626006462|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 CTTTCACTTC TGAGTCCCAG AGGTT
 R
 CCCAAGGCAC CCCTCTGACA TCCGG

  Submitted Frequency for ss3626006462 back to top
There is no frequency submission for ss3626006462.


  dbSNP summary of Genotypes for ss3626006462 back to top
No sufficient data to compute Hardy-weinberg probability for ss3626006462.


  Submitted individual genotype for ss3626006462 back to top
There is no individual genotype data for ss3626006462.