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Submitted SNP(ss) Details: ss3634035219           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpress-12v1_J_rs1403637-131_T_F_1857575070
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 AlleleT/C
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|ss3634035219|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 GAACACTCAA AGGAAGGAAT ACCTA
 Y
 GTGTAGTTGC ATACAACAGG TACAT

  Submitted Frequency for ss3634035219 back to top
There is no frequency submission for ss3634035219.


  dbSNP summary of Genotypes for ss3634035219 back to top
No sufficient data to compute Hardy-weinberg probability for ss3634035219.


  Submitted individual genotype for ss3634035219 back to top
There is no individual genotype data for ss3634035219.

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