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Submitted SNP(ss) Details: ss3633571437           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpress-12v1_J_rs6681049-131_T_R_1858018399
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|ss3633571437|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 AAGAACCTTT AGGACTGAGC ATGTC
 Y
 TTCTGTTTGC TTTAAGCTTT TAAGA

  Submitted Frequency for ss3633571437 back to top
There is no frequency submission for ss3633571437.


  dbSNP summary of Genotypes for ss3633571437 back to top
No sufficient data to compute Hardy-weinberg probability for ss3633571437.


  Submitted individual genotype for ss3633571437 back to top
There is no individual genotype data for ss3633571437.

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