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Submitted SNP(ss) Details: ss778436321           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni25Exome-8v1_A_rs1517342-131_B_F_1865444085
RefSNP(rs#)rs1517342
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 AlleleT/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|ss778436321|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 TAATATTCTC AAGGTGGGCA ATGTA
 Y
 ATTACACTCA AAGAAATAAA TGCAA

  Submitted Frequency for ss778436321 back to top
There is no frequency submission for ss778436321.


  dbSNP summary of Genotypes for ss778436321 back to top
No sufficient data to compute Hardy-weinberg probability for ss778436321.


  Submitted individual genotype for ss778436321 back to top
There is no individual genotype data for ss778436321.