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: ss1998445805           **clinically associated**
Submitter
HandleCLINVAR
Submitter SNP IDSCV000272934
RefSNP(rs#)rs771859047
Submitted Batch IDCLINVAR_2016-06-01
Submitted DateJun 02, 2016
Publication CitedN.D.
First entry to dbSNPJun 2 2016 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
genomic
MethodCLINICAL_SNP_SUBMISSION
Ascertainment SamplesizeN.D.
PopulationN.D.
Allele
Observed AlleleT/-
Ancestral AlleleN.D.
Allele OriginT:Germline :Germline
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|ss1998445805|allelePos=51|len=101|taxid=9606|alleles='T/-'|mol=Genomic
 TTAATTAAAT ATGTCATTTC ATTTCTTTTT CTTTTCTTTT TTTTTTTTTT
 N
 AGGACAAAAT GTTTCACTTT TGGGTAAATA CATTCTTCAT ACCAGGACCA

  Submitted Frequency for ss1998445805 back to top
There is no frequency submission for ss1998445805.


  dbSNP summary of Genotypes for ss1998445805 back to top
No sufficient data to compute Hardy-weinberg probability for ss1998445805.


  Submitted individual genotype for ss1998445805 back to top
There is no individual genotype data for ss1998445805.