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: ss2030297761           
Submitter
HandleJJLAB
Submitter SNP IDINDEL95
RefSNP(rs#)rs112791300
Submitted Batch IDWHOLE GENOME INDELS DISCOVERY
Submitted DateAug 30, 2016
Publication CitedN.D.
First entry to dbSNPAug 30 2016 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
GENOMIC
MethodILLUMINA HISEQ X TEN WHOLE GENOME SEQEUNCING
Ascertainment Samplesize96
PopulationN.D.
Allele
Observed AlleleGTGT/-
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassDIV
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|ss2030297761|allelePos=26|len=51|taxid=9606|alleles='GTGT/-'|mol=Genomic
 GAGAGAGCGA GGCGGCTGGA GGTGG
 N
 GTGACACCAG GTGACTTAGC GGCCC

  Submitted Frequency for ss2030297761 back to top
There is no frequency submission for ss2030297761.


  dbSNP summary of Genotypes for ss2030297761 back to top
No sufficient data to compute Hardy-weinberg probability for ss2030297761.


  Submitted individual genotype for ss2030297761 back to top
There is no individual genotype data for ss2030297761.