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Submitted SNP(ss) Details: ss11118905           
Submitter
HandleSC_SNP
Submitter SNP IDchr1.NT_032977.5_17649476
RefSNP(rs#)rs7354831
Submitted Batch IDCHR20_NA17119_200306
Submitted DateJul 03, 2003
Publication Cited[1] A linkage disequilibrium map of human chromosome 20
[2] SNPs detected by comparing chromosome and DNA specific sequences to NCBI Genomic Reference Sequence using SsahaSNP
[3] SSAHA: A Fast Search Method for Large DNA Databases
First entry to dbSNPJul 3 2003 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodCHR20_NA17119_200306
Ascertainment Samplesize2
PopulationN.D.
Allele
Observed AlleleC/T
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG Codec/t_g
Validation
Validation StatusbyFreq
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype Summarypopulation count: 13
Genotype SubmissionN.D.
HaplotypeN.D.
Comment
sequence:20SNP45080-1697g12.q1kposition:-494quality:40

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss11118905|allelePos=626|len=826|taxid=9606|alleles='C/T'|mol=Genomic
 ACTCTAATTT TACTGCCTGC TTTCTCAGGC CGTTTTTTGC CAAGtgtgtc aactgatagc
 ctctgagtag cagacaccaa gccaaaataa tatgtgaaaa caattttggt gaaaacgtct
 gtgaaagata aagaggagag gagcaggagt aggtggggag agatttcaaa ccacaaggca
 ggtgtgacac ttgtgaaaga aaagagggaa ggagaaaaaa tggggtagga agagctccag
 gctgcagtgc agctctgaga agtcttgacc aggtgattgg gaaggcctct tgcaaaggcc
 gtccattaga agaagcttct gtcaggcaga aatggcccag caatagtact ccactgtact
 caggtattgc ctgggagcag tgttggggag aggggagaga ggcctgagta tgaatgctgc
 agatctgtag gtacagccac tagctggagg ctgctggcca actacactcA GACGGCGTGT
 TCTCTAGAAG GGAGAGAGGC CTGAGTATGA ATGCTGCAGA TCTGTAGGTA CAGCCACTAG
 CTGGAGGCTG CTGGCCAACT ACACTCAGAC GGCGTGTTCT CTAGAAGGGA GATCTGAAGG
 GTACACCTAC ACAATCAAGT CTAAG
 Y
 GGCAGGAGCA GTAAATTAAG CCAAGGCCAG GAAGCCAGCT GGAAAATGGG ATGGGAGCCT
 GCAAAGGGGC TCCCATTGTA GGTAATAAGC AAAGGCATGC GCAAATTCTA CCTTTATTTA
 CATGTGCATG GCTGTAGTGG GTGGGTTTAG TGTATGGGTG TATGGACTGG TTTAATGTTA
 CAACAAGCAT GAAGGAGTTC

  Submitted Frequency for ss11118905 back to top
There is no frequency submission for ss11118905.


  dbSNP summary of Genotypes for ss11118905 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-CEU224224C=0.76785713
T=0.23214285C/C=0.57142860
C/T=0.39285713
T/T=0.03571429
Pr(chiSq=1.165,df=1)
=0.294
Genotype
Freq.
HapMap-HCB
EAST ASIA
8686C=0.51162791
T=0.48837209C/T=0.55813956
C/C=0.23255815
T/T=0.20930232
Pr(chiSq=0.587,df=1)
=0.479
Genotype
Freq.
HapMap-JPT172172C=0.54651165
T=0.45348838C/T=0.55813956
C/C=0.26744187
T/T=0.17441860
Pr(chiSq=1.366,df=1)
=0.251
Genotype
Freq.
HapMap-YRI226226T=0.85840708
C=0.14159292T/T=0.74336284
C/T=0.23008850
C/C=0.02654867
Pr(chiSq=0.323,df=1)
=0.584
Genotype
Freq.
HAPMAP-ASW9898T=0.69387758
C=0.30612245T/T=0.46938777
C/T=0.44897959
C/C=0.08163265
Pr(chiSq=0.158,df=1)
=0.752
Genotype
Freq.
HAPMAP-CHB8282T=0.54878050
C=0.45121950C/T=0.56097561
T/T=0.26829270
C/C=0.17073171
Pr(chiSq=0.722,df=1)
=0.403
Genotype
Freq.
HAPMAP-CHD170170C=0.54705882
T=0.45294118C/T=0.50588238
C/C=0.29411766
T/T=0.20000000
Pr(chiSq=0.037,df=1)
=1.000
Genotype
Freq.
HAPMAP-GIH176176C=0.72727275
T=0.27272728C/C=0.50000000
C/T=0.45454547
T/T=0.04545455
Pr(chiSq=1.872,df=1)
=0.200
Genotype
Freq.
HAPMAP-LWK180180T=0.77222222
C=0.22777778T/T=0.62222224
C/T=0.30000001
C/C=0.07777778
Pr(chiSq=1.951,df=1)
=0.200
Genotype
Freq.
HAPMAP-MEX100100C=0.67000002
T=0.33000001C/T=0.46000001
C/C=0.44000000
T/T=0.10000000
Pr(chiSq=0.081,df=1)
=1.000
Genotype
Freq.
HAPMAP-MKK286286T=0.53496504
C=0.46503496C/T=0.52447551
T/T=0.27272728
C/C=0.20279720
Pr(chiSq=0.419,df=1)
=0.527
Genotype
Freq.
HAPMAP-TSI176176C=0.75568181
T=0.24431819C/C=0.60227275
C/T=0.30681819
T/T=0.09090909
Pr(chiSq=2.516,df=1)
=0.150
Genotype
Freq.

  Submitted individual genotype for ss11118905 back to top
There is no individual genotype data for ss11118905.

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