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Submitted SNP(ss) Details: ss3028112979           
Submitter
HandleBIOINF_KMB_FNS_UNIBA
Submitter SNP ID16.40914G>A
RefSNP(rs#)rs117662806
Submitted Batch IDHorsa 1.0
Submitted DateJul 05, 2017
Publication Cited[1] Non invasive prenatal testing is a valuable source of population specific allelic frequencies
First entry to dbSNPJul 5 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodLOWCOVERAGENGS
Ascertainment Samplesize1548
PopulationN.D.
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|ss3028112979|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic
 TAATAATAAT AATAACAACA AGCTG
 R
 GCATGGTGCG CACCTGTAGT TCCAG

  Submitted Frequency for ss3028112979 back to top
There is no frequency submission for ss3028112979.


  dbSNP summary of Genotypes for ss3028112979 back to top
No sufficient data to compute Hardy-weinberg probability for ss3028112979.


  Submitted individual genotype for ss3028112979 back to top
There is no individual genotype data for ss3028112979.