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Submitted SNP(ss) Details: ss52077892           
Submitter
HandleSI_EXO
Submitter SNP IDNT_077913.3_496279
RefSNP(rs#)rs3766191
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 Samplesize40
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: 13
Genotype SubmissionN.D.
HaplotypeN.D.
Comment
ExoSeq_class:MHe2Estimated_frequency:.12Minor_allele:T

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss52077892|allelePos=401|len=801|taxid=9606|alleles='T/C'|mol=Genomic
 CAGCTCGGAA CGCAGCTTGA GTAATGCCGA CTTTATATCA GCACACCCAG TGCCCCCACG
 TTCCCGCTGG CCCAGGTCCC GGAGACCATG ATGGCACCCA CAGTGGACTT CGCAAAGGAG
 CGTGGGGACC CCGAAGGCCA GGCCACCCCT CAGAGGGGGG TCCCATGCTA AAGCAGACGG
 TGCCGGTGCC GCAGGGCGTC TGAGACCCAC GGTGGAGCCC GGGCCTGGCG TGCGGGAGGC
 GGCCACGACG GCGCCTTTCT CCCAGGAACT CCGGGAGGGA CCCCAGGACT CAGCGCCAGG
 GCAGCCTTGG CAGGTGCAGT GAGGCAGTGA CTTGTGGGGG TTAGATGTGG GCCTGCCCCA
 CGTGGGCAGG GATCAGCCAG GCATGGGGGT CCAGCGGATC
 Y
 GAGCGGGGCC ACAGAGCTCT GGAGGACTTT TCTGCACAAT GAATTTCTGC TTAAAAACAG
 AGATCAAGAG GAAGCTCTAT CCTGCAGCTC CGGAAATGGG TGGCTGCGTG CTTGGGGTCT
 CCGCCACGCG GGAGGACAGC CCAGAGGCAC CCTGGTCTCA GGCAGCTGGT TCCTAGGCTG
 TGTCCTCCCC ACTGGCCGGG CACCGGCTGG AACGGCACGA GGACCAGCCT CACTGTTCTC
 AGAGGGGTCT CGGGCCACTG GGTGTGGTGG TGCTGGAGGA GTCCTGCCCG CTGTGGGCTC
 TGGAGGGCAC GGCAGCAGAG CCCCTGGCTT TTCTAGGCAG AGCGGCACCT GCCCCATAGA
 TCGTGCCAGC TTTGGCTGCA GGCGCTGGGG CCTCACCGTG

  Submitted Frequency for ss52077892 back to top
There is no frequency submission for ss52077892.


  dbSNP summary of Genotypes for ss52077892 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=0.87610620
T=0.12389380C/C=0.76106197
C/T=0.23008850
T/T=0.00884956
Pr(chiSq=0.405,df=1)
=0.527
Genotype
Freq.
HapMap-HCB
EAST ASIA
8686C=0.82558137
T=0.17441860C/C=0.72093022
C/T=0.20930232
T/T=0.06976745
Pr(chiSq=3.210,df=1)
=0.100
Genotype
Freq.
HapMap-JPT170170C=0.86470586
T=0.13529412C/C=0.72941178
C/T=0.27058825
Pr(chiSq=0.525,df=1)
=0.479
Genotype
Freq.
HapMap-YRI226226C=0.76991153
T=0.23008850C/C=0.58407080
C/T=0.37168142
T/T=0.04424779
Pr(chiSq=0.272,df=1)
=0.655
Genotype
Freq.
HAPMAP-ASW9898C=0.76530612
T=0.23469388C/C=0.53061223
C/T=0.46938777
Pr(chiSq=1.909,df=1)
=0.200
Genotype
Freq.
HAPMAP-CHB8282C=0.85365856
T=0.14634146C/C=0.70731705
C/T=0.29268292
Pr(chiSq=0.327,df=1)
=0.584
Genotype
Freq.
HAPMAP-CHD170170C=0.90588236
T=0.09411765C/C=0.82352942
C/T=0.16470589
T/T=0.01176471
Pr(chiSq=0.099,df=1)
=1.000
Genotype
Freq.
HAPMAP-GIH176176C=0.81818181
T=0.18181819C/C=0.65909094
C/T=0.31818181
T/T=0.02272727
Pr(chiSq=0.424,df=1)
=0.527
Genotype
Freq.
HAPMAP-LWK180180C=0.78333336
T=0.21666667C/C=0.62222224
C/T=0.32222223
T/T=0.05555556
Pr(chiSq=0.232,df=1)
=0.655
Genotype
Freq.
HAPMAP-MEX100100C=0.92000002
T=0.08000000C/C=0.83999997
C/T=0.16000000
Pr(chiSq=0.058,df=1)
=1.000
Genotype
Freq.
HAPMAP-MKK286286C=0.85314685
T=0.14685315C/C=0.72027969
C/T=0.26573426
T/T=0.01398601
Pr(chiSq=0.523,df=1)
=0.479
Genotype
Freq.
HAPMAP-TSI176176C=0.82954544
T=0.17045455C/C=0.70454544
C/T=0.25000000
T/T=0.04545455
Pr(chiSq=1.184,df=1)
=0.294
Genotype
Freq.

  Submitted individual genotype for ss52077892 back to top
There is no individual genotype data for ss52077892.

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