NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss2019512120           
Submitter
HandleJJLAB
Submitter SNP IDSNP14675
RefSNP(rs#)rs7530315
Submitted Batch IDWHOLE GENOME SNPS DISCOVERY
Submitted DateAug 29, 2016
Publication CitedN.D.
First entry to dbSNPAug 29 2016 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
GENOMIC
MethodILLUMINA HISEQ X TEN WHOLE GENOME SEQEUNCING
Ascertainment Samplesize96
PopulationN.D.
Allele
Observed AlleleA/T
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss2019512120|allelePos=26|len=51|taxid=9606|alleles='A/T'|mol=Genomic
 CAGTCTGGAT GACAGAGCAA GACCC
 W
 ATCTCAAACA ATAATAAACA AAGAG

  Submitted Frequency for ss2019512120 back to top
There is no frequency submission for ss2019512120.


  dbSNP summary of Genotypes for ss2019512120 back to top
No sufficient data to compute Hardy-weinberg probability for ss2019512120.


  Submitted individual genotype for ss2019512120 back to top
There is no individual genotype data for ss2019512120.