NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss1917720789           
Submitter
HandleILLUMINA
Submitter SNP IDHumanExome-12v1-1_B_exm88-0_B_R_1921389782
RefSNP(rs#)rs149677938
Submitted Batch IDHumanExome-12v1-1
Submitted DateOct 16, 2015
Publication CitedN.D.
First entry to dbSNPOct 16 2015 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CUSTOMERIZED-CHIP
Ascertainment Samplesize242901
PopulationN.D.
Allele
Observed AlleleG/A
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|ss1917720789|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic
 GGCAAGAGGC TGGGCCGCTC CCCCC
 R
 TATCAGCAGC GACTGCTTTT CAGAG

  Submitted Frequency for ss1917720789 back to top
There is no frequency submission for ss1917720789.


  dbSNP summary of Genotypes for ss1917720789 back to top
No sufficient data to compute Hardy-weinberg probability for ss1917720789.


  Submitted individual genotype for ss1917720789 back to top
There is no individual genotype data for ss1917720789.