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: ss974769066           
Submitter
HandleEVA-GONL
Submitter SNP IDEVA-GONL_rs116801199
RefSNP(rs#)rs116801199
Submitted Batch IDrelease_5
Submitted DateApr 23, 2014
Publication CitedN.D.
First entry to dbSNPApr 23 2014 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodGATK
Ascertainment Samplesize1500
PopulationGONL
Allele
Observed AlleleG/T
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|ss974769066|allelePos=26|len=51|taxid=9606|alleles='G/T'|mol=Genomic
 AATGAATCTA ATAATGAGGA AACAT
 K
 AGAAAAAACC AAACTGAGGG ATATT

  Submitted Frequency for ss974769066 back to top
There is no frequency submission for ss974769066.


  dbSNP summary of Genotypes for ss974769066 back to top
No sufficient data to compute Hardy-weinberg probability for ss974769066.


  Submitted individual genotype for ss974769066 back to top
There is no individual genotype data for ss974769066.