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Submitted SNP(ss) Details: ss290850698           
Submitter
HandlePJP
Submitter SNP IDSNP_357056_chr10_62193782
RefSNP(rs#)rs2448334
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 AlleleC/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|ss290850698|allelePos=52|len=103|taxid=9606|alleles='C/G'|mol=Genomic
 ACATGAGAAT CGCTTGAACC TGGGAGGCAG AGGTTGCAGT GAACCAAGAT A
 S
 TGCCACTGCA CTCCAGTCTG GGCAACAGAG CTAGACTCTG TCTCAAAAAA C

  Submitted Frequency for ss290850698 back to top
There is no frequency submission for ss290850698.


  dbSNP summary of Genotypes for ss290850698 back to top
No sufficient data to compute Hardy-weinberg probability for ss290850698.


  Submitted individual genotype for ss290850698 back to top
There is no individual genotype data for ss290850698.