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Submitted SNP(ss) Details: ss3027582318           
Submitter
HandleBIOINF_KMB_FNS_UNIBA
Submitter SNP ID13.24459152G>C
RefSNP(rs#)rs4986819
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/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|ss3027582318|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic
 CAAAAATGAA GAGAAAGTTG TCTTA
 S
 TCTACGATCT TAAATTTCTA TCTGA

  Submitted Frequency for ss3027582318 back to top
There is no frequency submission for ss3027582318.


  dbSNP summary of Genotypes for ss3027582318 back to top
No sufficient data to compute Hardy-weinberg probability for ss3027582318.


  Submitted individual genotype for ss3027582318 back to top
There is no individual genotype data for ss3027582318.