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Submitted SNP(ss) Details: ss3772105660           
Submitter
HandleILLUMINA
Submitter SNP IDOmniExpressExome-8v1-1_C_rs2606418-131_T_F_1891264910
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmniExpressExome-8v1-1_C
Submitted DateJan 22, 2019
Publication CitedN.D.
First entry to dbSNPJan 22 2019 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize958178
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|ss3772105660|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 TATGAAAGTT AGGGCTGTGA ATATG
 R
 GGTGGCCTAC AGAAAGATGG AGGGA

  Submitted Frequency for ss3772105660 back to top
There is no frequency submission for ss3772105660.


  dbSNP summary of Genotypes for ss3772105660 back to top
No sufficient data to compute Hardy-weinberg probability for ss3772105660.


  Submitted individual genotype for ss3772105660 back to top
There is no individual genotype data for ss3772105660.