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Submitted SNP(ss) Details: ss3630507983           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni2.5-8v1_C_rs9424284-131_B_F_1865267016
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmni2.5-8v1_C
Submitted DateNov 28, 2017
Publication CitedN.D.
First entry to dbSNPNov 28 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize2379855
PopulationN.D.
Allele
Observed AlleleT/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|ss3630507983|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 AAGGATGTGA GGTGCACACT GGCTT
 Y
 GGGGAGGATG AGTTACACAG GGGGT

  Submitted Frequency for ss3630507983 back to top
There is no frequency submission for ss3630507983.


  dbSNP summary of Genotypes for ss3630507983 back to top
No sufficient data to compute Hardy-weinberg probability for ss3630507983.


  Submitted individual genotype for ss3630507983 back to top
There is no individual genotype data for ss3630507983.