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: ss52082698           
Submitter
HandleSI_EXO
Submitter SNP IDNT_004610.17_3801941
RefSNP(rs#)rs8064
Submitted Batch IDSI_EXO_20060323
Submitted DateMar 29, 2006
Publication Cited[1] A SNP-survey of human exons in 48 CEPH samples
First entry to dbSNPMar 29 2006 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodSI_EXOSEQ_1
Ascertainment Samplesize48
PopulationN.D.
Allele
Observed AlleleG/C
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: 13
Genotype SubmissionN.D.
HaplotypeN.D.
Comment
ExoSeq_class:MHe2Estimated_frequency:.15Minor_allele:G

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss52082698|allelePos=401|len=801|taxid=9606|alleles='G/C'|mol=Genomic
 GCTGGTGAAT TACTAAAAGA ACATGGCATC CTCTGTGTCG TGATGGTCTG TGAATGGTGA
 GGGTGGGAGT CAGGAGACAA GACAGCGCAG AGAGGGCTGG TTAGCCGGAA AAGGCCTCGG
 GCTTGGCAAA TGGAAGAACT TGAGTGAGAG TTCAGTCTGC AGTCCTCTGC TCACAGACAT
 CTGAAAAGTG AATGGCCAAG CTGGTCTAGT AGATGAGGCT GGACTGAGGA GGGGTAGGCC
 TGCATCCACA GAGAGGATCC AGGCCAAGGC ACTGGCTGTC AGTGGCAGAG TTTGGCTGTG
 ACCTTTGCCC CTAACACGAG GAACTCGTTT GAAGGGGGCA GCGTAGCATG TCTGATTTGC
 CACCTGGATG AAGGCAGACA TCAACATGGG TCAGCACGTT
 S
 AGTTACGGGA GTGGGAAATT ACATGAGGCC TGGGCCTCTG CGTTCCCAAG CTGTGCGTTC
 TGGACCAGCT ACTGAATTAT TAATCTCACT TAGCGAAAGT GACGGATGAG CAGTAAGTAA
 GTAAGTGTGG GGATTTAAAC TTGAGGGTTT CCCTCCTGAC TAGCCTCTCT TACAGGAATT
 GTGAAATATT AAATGCAAAT TTACAACTGC AGATGACGTA TGTGCCTTGA ACTGAATATT
 TGGCTTTAAG AATGATTCTT ATACTCTGAA GGTGAGAATA TTTTGTGGGC AGGTATCAAC
 ATTGGGGAAG AGATTTCATG TCTAACTAAC TAACTTTATA CATGATTTTT AGGAAGCTAT
 TGCCTAAATC AGCGTCAACA TGCAGTAAAG GTTGTCTTCA

  Submitted Frequency for ss52082698 back to top
There is no frequency submission for ss52082698.


  dbSNP summary of Genotypes for ss52082698 back to top

Population ID
 -Class
Total
Sample
(2N)
Founder
(2N)
Major
Allele
Freq.
Minor
Allele
Freq.
Genotype
Freq.
HWE Goodness of FitData
Source
HapMap-CEU226226C=0.82300884
G=0.17699115C/C=0.66371679
C/G=0.31858408
G/G=0.01769911
Pr(chiSq=0.989,df=1)
=0.343
Genotype
Freq.
HapMap-HCB
EAST ASIA
8686C=0.93023258
G=0.06976745C/C=0.86046511
C/G=0.13953489
Pr(chiSq=0.033,df=1)
=1.000
Genotype
Freq.
HapMap-JPT172172C=0.87209302
G=0.12790698C/C=0.74418604
C/G=0.25581396
Pr(chiSq=0.443,df=1)
=0.527
Genotype
Freq.
HAPMAP-ASW9898C=0.96938777
G=0.03061225C/C=0.93877554
C/G=0.06122449
Pr(chiSq=0.003,df=1)
=1.000
Genotype
Freq.
HAPMAP-CHB8282C=0.91463417
G=0.08536585C/C=0.82926828
C/G=0.17073171
Pr(chiSq=0.058,df=1)
=1.000
Genotype
Freq.
HAPMAP-CHD170170C=0.88235295
G=0.11764706C/C=0.76470590
C/G=0.23529412
Pr(chiSq=0.335,df=1)
=0.584
Genotype
Freq.
HAPMAP-GIH176176C=0.80113637
G=0.19886364C/C=0.63636363
C/G=0.32954547
G/G=0.03409091
Pr(chiSq=0.103,df=1)
=0.752
Genotype
Freq.
HAPMAP-MEX100100C=0.81000000
G=0.19000000C/C=0.62000000
C/G=0.38000000
Pr(chiSq=0.946,df=1)
=0.343
Genotype
Freq.
HAPMAP-MKK286286C=0.92657346
G=0.07342657C/C=0.86713284
C/G=0.11888112
G/G=0.01398601
Pr(chiSq=2.282,df=1)
=0.150
Genotype
Freq.
HAPMAP-TSI176176C=0.80113637
G=0.19886364C/C=0.63636363
C/G=0.32954547
G/G=0.03409091
Pr(chiSq=0.103,df=1)
=0.752
Genotype
Freq.

  Submitted individual genotype for ss52082698 back to top
There is no individual genotype data for ss52082698.

GENERAL: Contact Us | Homepage | Announcements |dbSNP Summary | Genome | FTP SERVER | Build History | Handle Request
DOCUMENTATION: FAQ | Searchable FAQ Archive | Overview | How to Submit | RefSNP Summary Info | Database Schema
SEARCH: Entrez SNP | Blast SNP | Batch Query | By Submitter |New Batches | Method | Population | Publication | Batch | Locus Info | Between Marker
NCBI: PubMed | Entrez | BLAST | OMIM | Taxonomy | Structure

Disclaimer     Privacy statement