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: ss161243664           
Submitter
HandleENSEMBL
Submitter SNP IDENSSNP205067
RefSNP(rs#)rs2606418
Submitted Batch ID2008-11-1
Submitted DateSep 24, 2009
Publication CitedN.D.
First entry to dbSNPSep 24 2009 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodENSEMBL-SSAHA
Ascertainment Samplesize2
PopulationENSEMBL_celera
Allele
Observed AlleleA/G
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG CodeN.D.
Validation
Validation StatusbyFreq
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype Summarypopulation count: 1
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss161243664|allelePos=102|len=203|taxid=9606|alleles='A/G'|mol=Genomic
 GTTGCTATGA TTTTTCTAAA ACTGCATAAC ACATCTAACC ACAGATCTAA GAAGTTCTAC
 AAACCCCAAA CAGGTCTATG AAAGTTAGGG CTGTGAATAT G
 R
 GGTGGCCTAC AGAAAGATGG AGGGAGTAAT CATCAGGGTG AGGACCATCT CCTACCCAAG
 TTCACTGGGC AAATGCTGTC TTTCTCATAT CTATACCCAT C

  Submitted Frequency for ss161243664 back to top
There is no frequency submission for ss161243664.


  dbSNP summary of Genotypes for ss161243664 back to top
No sufficient data to compute Hardy-weinberg probability for ss161243664.


  Submitted individual genotype for ss161243664 back to top
There is no individual genotype data for ss161243664.