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Submitted SNP(ss) Details: ss61705028           
Submitter
HandleSI_EXO
Submitter SNP IDNT_077569.2_6574486
RefSNP(rs#)rs9633765
Submitted Batch IDSI_EXO_20060629
Submitted DateJul 11, 2006
Publication Cited[1] A SNP-survey of human exons in 48 CEPH samples
First entry to dbSNPJul 11 2006 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodSI_EXOSEQ_1
Ascertainment Samplesize44
PopulationN.D.
Allele
Observed AlleleC/T
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: 12
Genotype SubmissionN.D.
HaplotypeN.D.
Comment
ExoSeq_class:SHW2Estimated_frequency:.38Minor_allele:C

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss61705028|allelePos=401|len=801|taxid=9606|alleles='C/T'|mol=Genomic
 TTTATAGCCA TAGTAGCCCT CTCTCCACCT CCCCTCACTT ATTCTATTTT TTTCTCCCTT
 TTCTAAGACC AAAAGTGAAG TTAAGAAGGT GGAAGGGAGA AGGAAGACAT TTTACAAAAA
 GGATACTCTT CTACTAAAAG ATAACCCCGC ACGGCATTTC ACACTTGCCT ACGTCACCCT
 GCTTTCCACG CACCTCCTCA GAGGGAGGGG CTGTTATTGT TCCTGTTTTA TGAAAAAAGC
 CGAGAGAGGC TACAGAACCT GTTTGATGTG ATAGCTAATT ATGGTCCGCG GAGCCTCAAA
 CCGAGTCGGG CCTGTGACTC CGAGCTGCGC TGCCTCGTAT TGATTGTCAT GCCTTTCTCC
 AAATACGCAC CAGATAAACT ATTGTATCTA TTCAGTATGA
 Y
 TGTTCTAACT CTGGCTTTGA GCTGTCGAGG TGGCTTCTAC CTTAGGTCTA GTTTTTGGAA
 AGGTGAAGCA GGAGTGGAAG CTCTCTAAGG GATACGAAAT CTGATTTTAT CCAAAGAAAT
 CACAGCAGCC TTTGAAAGAC ACATTCAGAT TTTCAAACAA ACAACAGACA ATTCAAAACC
 AGGCGCTCTG CTTATTCACT GAAACCGTAA GCTGCTGAAA CTCAGGGAAA AGCTTAAGAA
 ACTGGTCTTA AAGCTTCAGG CCAAACAATG CTTCAAATCA CATTTGAAGT AATCACTTAA
 AAACAGTAGA AAAATCAGTT ATCAATTACC TAAAACACTT ATACCCAATA AAATATTCCC
 ATGATGACAA GTGTCTGCTT CTTTCTAGAT GAGTGAAAGG

  Submitted Frequency for ss61705028 back to top
There is no frequency submission for ss61705028.


  dbSNP summary of Genotypes for ss61705028 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-CEU226226T=0.54424781
C=0.45575222C/T=0.48672566
T/T=0.30088496
C/C=0.21238938
Pr(chiSq=0.040,df=1)
=1.000
Genotype
Freq.
HapMap-HCB
EAST ASIA
8686C=0.56976742
T=0.43023255C/T=0.62790698
C/C=0.25581396
T/T=0.11627907
Pr(chiSq=3.389,df=1)
=0.100
Genotype
Freq.
HapMap-JPT172172T=0.55813956
C=0.44186047C/T=0.53488374
T/T=0.29069766
C/C=0.17441860
Pr(chiSq=0.613,df=1)
=0.439
Genotype
Freq.
HapMap-YRI226226T=0.59734511
C=0.40265486C/T=0.45132744
T/T=0.37168142
C/C=0.17699115
Pr(chiSq=0.431,df=1)
=0.527
Genotype
Freq.
HAPMAP-ASW9898T=0.67346936
C=0.32653061C/T=0.57142860
T/T=0.38775510
C/C=0.04081633
Pr(chiSq=4.388,df=1)
=0.050
Genotype
Freq.
HAPMAP-CHB8282C=0.57317072
T=0.42682928C/T=0.51219511
C/C=0.31707317
T/T=0.17073171
Pr(chiSq=0.090,df=1)
=1.000
Genotype
Freq.
HAPMAP-CHD170170C=0.60000002
T=0.40000001C/T=0.49411765
C/C=0.35294119
T/T=0.15294118
Pr(chiSq=0.074,df=1)
=1.000
Genotype
Freq.
HAPMAP-GIH176176T=0.71022725
C=0.28977272T/T=0.53409094
C/T=0.35227272
C/C=0.11363637
Pr(chiSq=1.829,df=1)
=0.200
Genotype
Freq.
HAPMAP-LWK180180T=0.64999998
C=0.34999999C/T=0.45555556
T/T=0.42222223
C/C=0.12222222
Pr(chiSq=0.000,df=1)
=1.000
Genotype
Freq.
HAPMAP-MEX100100T=0.58999997
C=0.41000000C/T=0.54000002
T/T=0.31999999
C/C=0.14000000
Pr(chiSq=0.675,df=1)
=0.439
Genotype
Freq.
HAPMAP-MKK286286T=0.62587410
C=0.37412587C/T=0.48251748
T/T=0.38461539
C/C=0.13286713
Pr(chiSq=0.132,df=1)
=0.752
Genotype
Freq.
HAPMAP-TSI176176T=0.65340906
C=0.34659091T/T=0.45454547
C/T=0.39772728
C/C=0.14772727
Pr(chiSq=1.307,df=1)
=0.254
Genotype
Freq.

  Submitted individual genotype for ss61705028 back to top
There is no individual genotype data for ss61705028.

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