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Submitted SNP(ss) Details: ss290498370           
Submitter
HandlePJP
Submitter SNP IDSNP_4728_chr1_3737179
RefSNP(rs#)rs4648417
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/T
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|ss290498370|allelePos=52|len=103|taxid=9606|alleles='C/T'|mol=Genomic
 AGGCAGGGCT TGCAGTGAGC CGAGATGGCA CCACTGCACC TCCAGCCTGG G
 Y
 GACAGAACGA GACTCCATCT CAAAAAAAAA AAAAAAAAAA GACAAAGAAA T

  Submitted Frequency for ss290498370 back to top
There is no frequency submission for ss290498370.


  dbSNP summary of Genotypes for ss290498370 back to top
No sufficient data to compute Hardy-weinberg probability for ss290498370.


  Submitted individual genotype for ss290498370 back to top
There is no individual genotype data for ss290498370.