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Submitted SNP(ss) Details: ss3673985047           
Submitter
HandleEGCUT_WGS
Submitter SNP IDVAR19723295
RefSNP(rs#)clustering in process
Submitted Batch IDE22
Submitted DateAug 28, 2018
Publication Cited[1] Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records
First entry to dbSNPAug 28 2018 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodPCR_FREE_WGS
Ascertainment Samplesize2240
PopulationEGCUT_WGS
Allele
Observed AlleleA/C
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|ss3673985047|allelePos=26|len=51|taxid=9606|alleles='A/C'|mol=Genomic
 TCTATTTAAA CCAGAAAGTA AATAA
 M
 TGTAATAAAA ATAGAAACAT ACCAA

  Submitted Frequency for ss3673985047 back to top
There is no frequency submission for ss3673985047.


  dbSNP summary of Genotypes for ss3673985047 back to top
No sufficient data to compute Hardy-weinberg probability for ss3673985047.


  Submitted individual genotype for ss3673985047 back to top
There is no individual genotype data for ss3673985047.