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: ss3625523718           
Submitter
HandleILLUMINA
Submitter SNP IDNeuro_Consortium_20013217_A2_rs2842910-131_B_F_1891377466
RefSNP(rs#)clustering in process
Submitted Batch IDNeuro_Consortium_20013217_A2
Submitted DateNov 06, 2017
Publication CitedN.D.
First entry to dbSNPNov 6 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize486137
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|ss3625523718|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 AGTCTAAAGT GTTGAGATTG TGCAA
 Y
 GCTCGTCCAG GGTCACTTTG TGAGA

  Submitted Frequency for ss3625523718 back to top
There is no frequency submission for ss3625523718.


  dbSNP summary of Genotypes for ss3625523718 back to top
No sufficient data to compute Hardy-weinberg probability for ss3625523718.


  Submitted individual genotype for ss3625523718 back to top
There is no individual genotype data for ss3625523718.