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Submitted SNP(ss) Details: ss71644655           
Submitter
HandleSI_EXO
Submitter SNP IDNT_032977.8_55533465
RefSNP(rs#)rs709766
Submitted Batch IDSI_EXO_20070501
Submitted DateMay 07, 2007
Publication CitedN.D.
First entry to dbSNPMay 7 2007 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodSI_EXOSEQ_1
Ascertainment Samplesize46
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
Warning: Incomplete sequence coverage - frequency may be inaccurate.ExoSeq_class:SHW2Estimated_frequency:.3478Minor_allele:T

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss71644655|allelePos=401|len=801|taxid=9606|alleles='C/T'|mol=Genomic
 AGAGCCACTC TCTCACTAGA GTTTTCTAAC CTTTCTACCC TGTAGATCTC CTCTCCACTC
 CAGGAGTGCC TGGCTCAGTA TTCAGCAAGC AACAAAACAG ACACAGATCC TGTCCTCACA
 GAGCTTCCCT TCCATGGTTT TCAGGAACAC TAATTTCATA GTCTTTTTGT TATAAACATT
 GTAACATGCT CCCAAAATAA CTACAATTTG TTTCCACTGA GGGGTGGGTT GGGGAATACC
 TGGGTCCCCT TGAGAACATA CTCACTGTCA CTCGTATGGC CAATGTGCAC AATAAAATTA
 AGCAAAAGCA GCTTTTAGTC CAGAGGCAGA ACTCTGAGAA TAGACTCTCT ACGCACCTTG
 CTTATAGATA GCTATAAAAT TAGACTTTTA ACTGTCTTAA
 Y
 ATTATTTTCT CGCCATGATC TTAATCTCTT TTCTCATTCT TTCATGAATT TGCTGGGTTT
 ACTTTAGTTA ATGCTGGAGA GCCCAGATGA CATCTTCTGC TTCAAGTTCT GTCCGAGTGA
 TCCTAATATC ATTGCTGGAG GCTGTATCAA TGGGCAGGTA CTTAACAGAA TTTTTTTCAG
 CTATGTATTA ATGTAGACAA CCTTTGGTAA TAAGTTTTGA CTTGGCAGTT CCTTGGACTT
 AAGGATTCAA TTCAGCAGAA GGAAGGCATG CCAATTGTGT GCCAGACACC ACACCAGGAA
 GCAGGGTATA GAGACGTGTT ACACACGGTA TCAGCTCCTG AGGTGTTCAC GGGGTAACCC
 AGCTTCAAAA CTGAAACAGA ATTGGGTGAA ATCTATTTGT

  Submitted Frequency for ss71644655 back to top
There is no frequency submission for ss71644655.


  dbSNP summary of Genotypes for ss71644655 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=0.59292036
T=0.40707964C/T=0.42477876
C/C=0.38053098
T/T=0.19469027
Pr(chiSq=1.629,df=1)
=0.251
Genotype
Freq.
HapMap-HCB
EAST ASIA
8484T=0.54761904
C=0.45238096C/T=0.57142860
T/T=0.26190478
C/C=0.16666667
Pr(chiSq=0.987,df=1)
=0.343
Genotype
Freq.
HapMap-JPT172172T=0.59883720
C=0.40116280C/T=0.45348838
T/T=0.37209302
C/C=0.17441860
Pr(chiSq=0.271,df=1)
=0.655
Genotype
Freq.
HapMap-YRI226226C=0.72566372
T=0.27433628C/C=0.55752212
C/T=0.33628318
T/T=0.10619469
Pr(chiSq=2.728,df=1)
=0.100
Genotype
Freq.
HAPMAP-ASW9696C=0.66666669
T=0.33333334C/T=0.50000000
C/C=0.41666666
T/T=0.08333334
Pr(chiSq=0.750,df=1)
=0.403
Genotype
Freq.
HAPMAP-CHB8080T=0.61250001
C=0.38749999C/T=0.52499998
T/T=0.34999999
C/C=0.12500000
Pr(chiSq=0.449,df=1)
=0.527
Genotype
Freq.
HAPMAP-CHD170170T=0.57058823
C=0.42941177C/T=0.45882353
T/T=0.34117648
C/C=0.20000000
Pr(chiSq=0.345,df=1)
=0.584
Genotype
Freq.
HAPMAP-GIH174174C=0.53448278
T=0.46551725C/T=0.54022986
C/C=0.26436782
T/T=0.19540229
Pr(chiSq=0.638,df=1)
=0.439
Genotype
Freq.
HAPMAP-LWK180180C=0.66111112
T=0.33888888C/C=0.44444445
C/T=0.43333334
T/T=0.12222222
Pr(chiSq=0.098,df=1)
=1.000
Genotype
Freq.
HAPMAP-MEX9494C=0.55319148
T=0.44680852C/T=0.51063830
C/C=0.29787233
T/T=0.19148937
Pr(chiSq=0.051,df=1)
=1.000
Genotype
Freq.
HAPMAP-MKK286286C=0.58741260
T=0.41258740C/T=0.51748252
C/C=0.32867134
T/T=0.15384616
Pr(chiSq=0.653,df=1)
=0.439
Genotype
Freq.
HAPMAP-TSI176176C=0.55681819
T=0.44318181C/T=0.38636363
C/C=0.36363637
T/T=0.25000000
Pr(chiSq=4.150,df=1)
=0.050
Genotype
Freq.

  Submitted individual genotype for ss71644655 back to top
There is no individual genotype data for ss71644655.

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