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Submitted SNP(ss) Details: ss3635041090           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpressExome-8v1-2_A_exm513002-0_B_F_1921938281
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 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|ss3635041090|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 AGCCTTGTCA ATGGATCCAC TGAGC
 Y
 CGGAGAGAGC AACTCCGCAA TTTTA

  Submitted Frequency for ss3635041090 back to top
There is no frequency submission for ss3635041090.


  dbSNP summary of Genotypes for ss3635041090 back to top
No sufficient data to compute Hardy-weinberg probability for ss3635041090.


  Submitted individual genotype for ss3635041090 back to top
There is no individual genotype data for ss3635041090.

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