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Submitted SNP(ss) Details: ss3634301838           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpressExome-8v1-2_A_exm88-0_B_R_1921389782
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmniExpressExome-8v1-2_A
Submitted DateDec 07, 2017
Publication CitedN.D.
First entry to dbSNPDec 7 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize964193
PopulationN.D.
Allele
Observed AlleleG/A
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|ss3634301838|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic
 GGCAAGAGGC TGGGCCGCTC CCCCC
 R
 TATCAGCAGC GACTGCTTTT CAGAG

  Submitted Frequency for ss3634301838 back to top
There is no frequency submission for ss3634301838.


  dbSNP summary of Genotypes for ss3634301838 back to top
No sufficient data to compute Hardy-weinberg probability for ss3634301838.


  Submitted individual genotype for ss3634301838 back to top
There is no individual genotype data for ss3634301838.