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Submitted SNP(ss) Details: ss291564910           
Submitter
HandlePJP
Submitter SNP IDSNP_1071268_chr13_28123001
RefSNP(rs#)rs7335242
Submitted Batch IDNSMB2011_SNP
Submitted DateJan 21, 2011
Publication Cited[1] Impact of chromatin structure on sequence variability in the human genome
First entry to dbSNPJan 21 2011 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodTRACESALIGNMENT
Ascertainment SamplesizeN.D.
PopulationN.D.
Allele
Observed AlleleA/G
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Homozygote Detected
PCR Confirmed
In Expressed Sequence
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss291564910|allelePos=52|len=103|taxid=9606|alleles='A/G'|mol=Genomic
 GATGACATTT TTCACAACGA CAAAATCGCC TAATGCTGCA TTTCTCGGAA C
 R
 TATCCCTATT GTTAAGAGAC GTATGACTAT ATTCTTTCTG TAATAGTGAT A

  Submitted Frequency for ss291564910 back to top
There is no frequency submission for ss291564910.


  dbSNP summary of Genotypes for ss291564910 back to top
No sufficient data to compute Hardy-weinberg probability for ss291564910.


  Submitted individual genotype for ss291564910 back to top
There is no individual genotype data for ss291564910.

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