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Submitted SNP(ss) Details: ss2136849438           **clinically associated**
Submitter
HandleCLINVAR
Submitter SNP IDSCV000337555
RefSNP(rs#)rs397515332
Submitted Batch IDCLINVAR_2016-11-30
Submitted DateDec 04, 2016
Publication CitedN.D.
First entry to dbSNPDec 4 2016 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
genomic
MethodCLINICAL_SNP_SUBMISSION
Ascertainment SamplesizeN.D.
PopulationN.D.
Allele
Observed AlleleC/G
Ancestral AlleleN.D.
Allele OriginG:Germline A:Germline C: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|ss2136849438|allelePos=51|len=101|taxid=9606|alleles='C/G'|mol=Genomic
 GAAATTTTAG GGACTAAAAC AATTTTTACT TACGGGTCCA CCCTCATCAC
 S
 AGGATAGCCT CGGTAGCCGT CTTCTCCAGG AATACCCTGA AACAAAGTAA

  Submitted Frequency for ss2136849438 back to top
There is no frequency submission for ss2136849438.


  dbSNP summary of Genotypes for ss2136849438 back to top
No sufficient data to compute Hardy-weinberg probability for ss2136849438.


  Submitted individual genotype for ss2136849438 back to top
There is no individual genotype data for ss2136849438.