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Submitted SNP(ss) Details: ss3641278513           
Submitter
HandleILLUMINA
Submitter SNP IDHumanCytoSNP-12v2_H_rs12025301-131_T_F_1857977832
RefSNP(rs#)clustering in process
Submitted Batch IDHumanCytoSNP-12v2_H
Submitted DateDec 29, 2017
Publication CitedN.D.
First entry to dbSNPDec 29 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize300739
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|ss3641278513|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 AAGTACATAC AAATGTGGGC CCCTC
 R
 AAGAAGCCAC CTTTATATGC AGTCA

  Submitted Frequency for ss3641278513 back to top
There is no frequency submission for ss3641278513.


  dbSNP summary of Genotypes for ss3641278513 back to top
No sufficient data to compute Hardy-weinberg probability for ss3641278513.


  Submitted individual genotype for ss3641278513 back to top
There is no individual genotype data for ss3641278513.

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