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Submitted SNP(ss) Details: ss71648569           
Submitter
HandleSI_EXO
Submitter SNP IDNT_004350.18_500047
RefSNP(rs#)rs3737728
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 Samplesize34
PopulationN.D.
Allele
Observed AlleleG/A
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:MHo2Estimated_frequency:.3Minor_allele:A

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss71648569|allelePos=401|len=801|taxid=9606|alleles='G/A'|mol=Genomic
 GAGGTTCTGG GCCCCGAGGA AGGCCCCTTG GTGCTTCGAC CCTTCAAATC CACACACGGC
 TGTTTCCGGG AAGTGACGGG CCTTCTCACA CCGGGACCCA AAAGCCACAG GACAGGCCCT
 GCTCCCTCCC GGCCTCTGCC AGCCTGCTCT GGCCTGGGAC ACTCCAGTCT CAGGCCCATC
 TCCACGGCTG GATGCCGCCT GCCCTGTGCC CTCCCGTGGG GCAGGTGCTG GTCCGGGAGA
 TACCTTTGTT TCTTCTGTAG CAGGCCCTGG GGAGTTTACT GGAGCGCTTG AGGTAGAAGA
 ACCCAGCTAC GGAGAGGATG AGGCCGGAGC TAATGAAGAA CGTGCCCAGG AAGAGGGAGG
 CGGCCACGCG CGGAGCCCCT GCAAACAGAC ACCGCTGAGC
 R
 GACGGGCAGG ACGGTGGCCC TGGCTCCTCG CCTGGCCCCC GGTGCCCCCT GCACATGGCA
 GATGCGCTGC TCTCTGAACA TGCCTGAGCC TCACGGGACC GGCTGTGGGT GCCGAGGGCT
 CTGCACATGG GCCTGGGTCA TCCCTGCAGG CTCAGCCATG CCTGGGCATC TGGCCGCGGG
 GTCTGGGAAA GTTACCACCT GCCCCGGCCT CAGCTTCTCT CAGGAGCTCG GATGTTGGGA
 GCGTTACAGG GGCTGACCCT GGCCGGGCTC TGCGGAAACA CCTCTCCGAT TCCAGTTGCC
 CCTGAAAGCC AGGGGGTTCT CAGCCTTGTT CCTTCCTCCG GGCTCAGCAC AGGCCCTGGG
 GCCCCCACAC AGGGCAGAGC CTCAAGCTGG CAGCAGGTGC

  Submitted Frequency for ss71648569 back to top
There is no frequency submission for ss71648569.


  dbSNP summary of Genotypes for ss71648569 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-CEU226226G=0.73451328
A=0.26548672G/G=0.52212387
A/G=0.42477876
A/A=0.05309734
Pr(chiSq=0.898,df=1)
=0.371
Genotype
Freq.
HapMap-HCB
EAST ASIA
8686G=0.94186044
A=0.05813954G/G=0.88372093
A/G=0.11627907
Pr(chiSq=0.018,df=1)
=1.000
Genotype
Freq.
HapMap-JPT172172G=0.93604654
A=0.06395349G/G=0.87209302
A/G=0.12790698
Pr(chiSq=0.050,df=1)
=1.000
Genotype
Freq.
HapMap-YRI226226G=0.84955752
A=0.15044248G/G=0.72566372
A/G=0.24778761
A/A=0.02654867
Pr(chiSq=0.106,df=1)
=0.752
Genotype
Freq.
HAPMAP-ASW9898G=0.74489796
A=0.25510204G/G=0.51020408
A/G=0.46938777
A/A=0.02040816
Pr(chiSq=2.708,df=1)
=0.150
Genotype
Freq.
HAPMAP-CHB8282G=0.89024389
A=0.10975610G/G=0.80487806
A/G=0.17073171
A/A=0.02439024
Pr(chiSq=0.654,df=1)
=0.439
Genotype
Freq.
HAPMAP-CHD170170G=0.90588236
A=0.09411765G/G=0.82352942
A/G=0.16470589
A/A=0.01176471
Pr(chiSq=0.099,df=1)
=1.000
Genotype
Freq.
HAPMAP-GIH176176G=0.73863637
A=0.26136363G/G=0.52272725
A/G=0.43181819
A/A=0.04545455
Pr(chiSq=1.234,df=1)
=0.273
Genotype
Freq.
HAPMAP-LWK180180G=0.77222222
A=0.22777778G/G=0.57777780
A/G=0.38888890
A/A=0.03333334
Pr(chiSq=1.001,df=1)
=0.317
Genotype
Freq.
HAPMAP-MEX100100G=0.75999999
A=0.23999999G/G=0.54000002
A/G=0.44000000
A/A=0.02000000
Pr(chiSq=2.125,df=1)
=0.150
Genotype
Freq.
HAPMAP-MKK284284G=0.63028169
A=0.36971831A/G=0.51408452
G/G=0.37323943
A/A=0.11267605
Pr(chiSq=1.508,df=1)
=0.251
Genotype
Freq.
HAPMAP-TSI176176G=0.70454544
A=0.29545453G/G=0.50000000
A/G=0.40909091
A/A=0.09090909
Pr(chiSq=0.027,df=1)
=1.000
Genotype
Freq.

  Submitted individual genotype for ss71648569 back to top
There is no individual genotype data for ss71648569.

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