NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss3727485682           
Submitter
HandleACPOP
Submitter SNP ID1:1051087
RefSNP(rs#)clustering in process
Submitted Batch IDACPOP
Submitted DateNov 09, 2018
Publication Cited[1] A whole-genome sequenced control population in northern Sweden reveals subregional genetic differences.
First entry to dbSNPNov 9 2018 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodWGS_ILLUMINA
Ascertainment Samplesize600
PopulationACPOP
Allele
Observed AlleleG/A
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|ss3727485682|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic
 GTGAGAGGGA CCCTGGGTGG TGGCA
 R
 TGACCCCACA GGCTTAGGGG CCTTC

  Submitted Frequency for ss3727485682 back to top
There is no frequency submission for ss3727485682.


  dbSNP summary of Genotypes for ss3727485682 back to top
No sufficient data to compute Hardy-weinberg probability for ss3727485682.


  Submitted individual genotype for ss3727485682 back to top
There is no individual genotype data for ss3727485682.