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: ss68404361           
Submitter
HandleCSHL-HAPMAP
Submitter SNP IDperlegen:assay:25761.4779534:1
RefSNP(rs#)rs4952
Submitted Batch IDnewSsNewProbe-HAPMAP-PERLEGEN
Submitted DateJan 11, 2007
Publication CitedN.D.
First entry to dbSNPJan 11 2007 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
NA
MethodHAPMAP-PERLEGEN
Ascertainment Samplesize8
PopulationN.D.
Allele
Observed AlleleC/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|ss68404361|allelePos=51|len=101|taxid=9606|alleles='C/T'|mol=NA
 AATGTCGACA GAAAAGACTT CTTCGATAAC GGAGAATGGG AAATACTGAA
 Y
 GCAAAGGGGA TGAAGGGGAA CAGAAGGGAC GGCGTGTACT CCTATCCCTT

  Submitted Frequency for ss68404361 back to top
There is no frequency submission for ss68404361.


  dbSNP summary of Genotypes for ss68404361 back to top
No sufficient data to compute Hardy-weinberg probability for ss68404361.


  Submitted individual genotype for ss68404361 back to top
There is no individual genotype data for ss68404361.