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: ss836188029           **clinically associated**
Submitter
HandleEGL
Submitter SNP IDSCV000058323
RefSNP(rs#)rs200338097
Submitted Batch IDEGL_2013-09-19
Submitted DateOct 18, 2013
Publication CitedN.D.
First entry to dbSNPOct 18 2013 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
genomic
MethodLSDB_SNP_SUBMISSION
Ascertainment SamplesizeN.D.
PopulationN.D.
Allele
Observed AlleleA/T
Ancestral AlleleN.D.
Allele OriginT:Germline A:Germline
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|ss836188029|allelePos=51|len=101|taxid=9606|alleles='A/T'|mol=Genomic
 GGTAAGTAAT GTTAGTTTAT CTTGTGATAT GGAATTTAAC TAATTAATAG
 W
 TAGGTAAAGT TTTCCAGTCT TTCTAATTCT CCATATAGTT GAATTGTACT

  Submitted Frequency for ss836188029 back to top
There is no frequency submission for ss836188029.


  dbSNP summary of Genotypes for ss836188029 back to top
No sufficient data to compute Hardy-weinberg probability for ss836188029.


  Submitted individual genotype for ss836188029 back to top
There is no individual genotype data for ss836188029.