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Submitted SNP(ss) Details: ss61705032           
Submitter
HandleSI_EXO
Submitter SNP IDNT_017696.14_1339063
RefSNP(rs#)rs10857472
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 Samplesize47
PopulationN.D.
Allele
Observed AlleleA/G
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:A

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss61705032|allelePos=401|len=801|taxid=9606|alleles='A/G'|mol=Genomic
 GTCACAGGAG GGAAAGCCCT GCCCGGAGGA CTTGGAGCAG ACACAGCAAA GGCCGCTGTG
 CCCCAGAGAG AGGCCCCGAC ACAATTTCCC CGTGGTCCGT TCCCTGCCCC CTCCCGTGCA
 CCGCCACTCC GTGTCCGGCT TCTCGGAGCC TGTCGGGAGG CGGCCCGGGG GCCCCCAGTC
 CCTCACACCC CTGCCCGCGT ACCCCGCCAC CCAGAAGGTC CTCCAGGATC CGCAGTCCGG
 GGAGTACTTT GTCTTCGACT TGCCACTCCA GGTGAAAATC AAGACCTTCT ATGACCCAGA
 GACGGGCAAG TATGTCAAGG TCTCCATCCC GTCCTCCGAG GGGGCCTCCC CAGAGCCGCC
 CCCACCGGAC GCCCTGGCCG CTCCCTATGT GCTGTACCCC
 R
 GCTTCCAGCC AGTGCCCGTG ACGGCCTTGA TGCCGCTGCG CTGCTCCTCT CAGCTCTCCG
 CGCCCACCTT CCTCAGGCAG GGCCCTCGTG CCTCCGCGGC CCGCGCCAGG ACCCAGAGTG
 TCCACGAGTC TGGACTACAG CTGGACCCAG GGCCTCACGG TGACTGCACC CCGCACTCTG
 CAGGCCAGCG CCCTCATGGT CCTCCCCAGA GCCCAGGAGA GGAGGGTGTA GAAGCTCCAG
 GCCTGGGCAT CATCTCCACT GATGACCTAG AGGACTTTGC CACAGAAGGC ATTTCTTGAG
 TTACTGCAGG CTGTCCCCCA CCCCCAGATG AACCCAGAGG AGCTTACTTC CCCCTCCCCC
 AAAACAAGCA ACACACACAC ACACACACAC ACACACACAC

  Submitted Frequency for ss61705032 back to top
There is no frequency submission for ss61705032.


  dbSNP summary of Genotypes for ss61705032 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=0.56194693
A=0.43805310A/G=0.43362832
G/G=0.34513274
A/A=0.22123894
Pr(chiSq=1.606,df=1)
=0.251
Genotype
Freq.
HapMap-HCB
EAST ASIA
8686G=0.79069769
A=0.20930232G/G=0.60465115
A/G=0.37209302
A/A=0.02325581
Pr(chiSq=0.663,df=1)
=0.439
Genotype
Freq.
HapMap-JPT172172G=0.77325583
A=0.22674419G/G=0.60465115
A/G=0.33720931
A/A=0.05813954
Pr(chiSq=0.127,df=1)
=0.752
Genotype
Freq.
HapMap-YRI226226G=0.75663716
A=0.24336283G/G=0.55752212
A/G=0.39823008
A/A=0.04424779
Pr(chiSq=0.748,df=1)
=0.403
Genotype
Freq.
HAPMAP-ASW9898G=0.79591835
A=0.20408164G/G=0.63265306
A/G=0.32653061
A/A=0.04081633
Pr(chiSq=0.001,df=1)
=1.000
Genotype
Freq.
HAPMAP-CHB8282G=0.82926828
A=0.17073171G/G=0.70731705
A/G=0.24390244
A/A=0.04878049
Pr(chiSq=0.788,df=1)
=0.403
Genotype
Freq.
HAPMAP-CHD170170G=0.82941175
A=0.17058824G/G=0.68235296
A/G=0.29411766
A/A=0.02352941
Pr(chiSq=0.132,df=1)
=0.752
Genotype
Freq.
HAPMAP-GIH176176A=0.52272725
G=0.47727272A/G=0.45454547
A/A=0.29545453
G/G=0.25000000
Pr(chiSq=0.697,df=1)
=0.439
Genotype
Freq.
HAPMAP-LWK180180G=0.80555558
A=0.19444445G/G=0.63333333
A/G=0.34444445
A/A=0.02222222
Pr(chiSq=0.891,df=1)
=0.371
Genotype
Freq.
HAPMAP-MEX9898G=0.65306121
A=0.34693879A/G=0.44897959
G/G=0.42857143
A/A=0.12244898
Pr(chiSq=0.004,df=1)
=1.000
Genotype
Freq.
HAPMAP-MKK286286G=0.70629370
A=0.29370630G/G=0.50349653
A/G=0.40559441
A/A=0.09090909
Pr(chiSq=0.072,df=1)
=1.000
Genotype
Freq.
HAPMAP-TSI174174G=0.52873564
A=0.47126436A/G=0.41379312
G/G=0.32183909
A/A=0.26436782
Pr(chiSq=2.505,df=1)
=0.150
Genotype
Freq.

  Submitted individual genotype for ss61705032 back to top
There is no individual genotype data for ss61705032.

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