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: ss68103670           
Submitter
HandleILLUMINA
Submitter SNP IDHumanHap250Sv1.0_rs11202607
RefSNP(rs#)rs11202607
Submitted Batch IDHumanHap250Sv1.0
Submitted DateDec 06, 2006
Publication CitedN.D.
First entry to dbSNPDec 6 2006 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodINFINIUM-II
Ascertainment Samplesize270
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|ss68103670|allelePos=51|len=101|taxid=9606|alleles='C/T'|mol=Genomic
 TAGTTATAAA TATTGTTCTT TGTTACAATT TCGGGCACCG CATATTAAAA
 Y
 GTAACTTTAT TGTTCCAATA TGTAACATGG AGGGCCAGGT CATAAATAAT

  Submitted Frequency for ss68103670 back to top
There is no frequency submission for ss68103670.


  dbSNP summary of Genotypes for ss68103670 back to top
No sufficient data to compute Hardy-weinberg probability for ss68103670.


  Submitted individual genotype for ss68103670 back to top
There is no individual genotype data for ss68103670.