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Submitted SNP(ss) Details: ss778342335           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni25Exome-8v1_A_rs12119601-131_T_F_1865547305
RefSNP(rs#)rs12119601
Submitted Batch IDHumanOmni25Exome-8v1_A
Submitted DateMay 30, 2013
Publication CitedN.D.
First entry to dbSNPMay 30 2013 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize2
PopulationN.D.
Allele
Observed AlleleG/C
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss778342335|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic
 TGTTCTATCC TAATAGTACC ACTAT
 S
 TACACAGTTG CTCAAGCCAA AAATC

  Submitted Frequency for ss778342335 back to top
There is no frequency submission for ss778342335.


  dbSNP summary of Genotypes for ss778342335 back to top
No sufficient data to compute Hardy-weinberg probability for ss778342335.


  Submitted individual genotype for ss778342335 back to top
There is no individual genotype data for ss778342335.