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Submitted SNP(ss) Details: ss68756308           
Submitter
HandlePERLEGEN
Submitter SNP IDPGP01839173
RefSNP(rs#)rs3748596
Submitted Batch IDPGP_29-JAN-2007
Submitted DateJan 30, 2007
Publication CitedN.D.
First entry to dbSNPJan 30 2007 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodPERLEGEN-600K
Ascertainment Samplesize1
PopulationN.D.
Allele
Observed AlleleT/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: 4
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss68756308|allelePos=65|len=129|taxid=9606|alleles='T/C'|mol=Genomic
 AAGTGTCCTT CTTGTGCCGG CAGACTCTGC TGAGGACCAG GAAAGCCAGC
 ACCCGCAGAG ACTC
 Y
 TCCCCAGTGC TCCA
 TACGATCACC ATTCTCTGCA GAAGGTCAGA CGTCACTGGT GGCCCCCCAG

  Submitted Frequency for ss68756308 back to top
There is no frequency submission for ss68756308.


  dbSNP summary of Genotypes for ss68756308 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-CEU120120C=0.94166666
T=0.05833333C/C=0.88333333
C/T=0.11666667
Pr(chiSq=0.026,df=1)
=1.000
Genotype
Freq.
HapMap-HCB
EAST ASIA
9090C=0.94444442
T=0.05555556C/C=0.88888890
C/T=0.11111111
Pr(chiSq=0.017,df=1)
=1.000
Genotype
Freq.
HapMap-JPT9090C=0.96666664
T=0.03333334C/C=0.93333334
C/T=0.06666667
Pr(chiSq=0.004,df=1)
=1.000
Genotype
Freq.
HapMap-YRI120120C=0.89166665
T=0.10833333C/C=0.78333336
C/T=0.21666667
Pr(chiSq=0.182,df=1)
=0.752
Genotype
Freq.

  Submitted individual genotype for ss68756308 back to top
There is no individual genotype data for ss68756308.