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: ss1599427728           
Submitter
HandleEVA_UK10K_ALSPAC
Submitter SNP IDEVA_UK10K_ALSPAC_1_3747319_53993
RefSNP(rs#)rs4648417
Submitted Batch IDEVA_UK10K_ALSPAC
Submitted DateMar 04, 2015
Publication CitedN.D.
First entry to dbSNPMar 4 2015 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodPARENT_OFFSPRING_WGS
Ascertainment Samplesize3854
PopulationPARENT AND CHILD COHORT
Allele
Observed AlleleC/T
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|ss1599427728|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 GGCACCACTG CACCTCCAGC CTGGG
 Y
 GACAGAACGA GACTCCATCT CAAAA

  Submitted Frequency for ss1599427728 back to top
There is no frequency submission for ss1599427728.


  dbSNP summary of Genotypes for ss1599427728 back to top
No sufficient data to compute Hardy-weinberg probability for ss1599427728.


  Submitted individual genotype for ss1599427728 back to top
There is no individual genotype data for ss1599427728.