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Submitted SNP(ss) Details: ss50017592           
Submitter
HandleDEVINE_LAB
Submitter SNP IDINDEL_GP35_WGS_197492
RefSNP(rs#)rs34302627
Submitted Batch IDEMORY_INDEL_GP35_WGS
Submitted DateJan 24, 2006
Publication Cited[1] An initial map of insertion and deletion (INDEL) variation in the human genome
First entry to dbSNPJan 24 2006 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodMETHOD_WGS
Ascertainment Samplesize2
PopulationN.D.
Allele
Observed Allele-/TGT
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassDIV
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|ss50017592|allelePos=401|len=801|taxid=9606|alleles='-/TGT'|mol=Genomic
 ATGGGCCAAG GAGGACAGGA AAGCTCTCTG ACCCACAGGT ATCTGTGTTT AATATTCCAT
 CCTAGTTTCT CTTTCTCTCT CTCCTCTTTC ACTTCTCTCT CTCTGTCTCT CTTTCTCTCT
 CTCTCTCTCT TTCTTTTTGA CACAGGGTCT TGCTCTGTCG CCTAGGCTAG AGTATAGCAG
 TGCAATCATG GCTCACTGCA GCCTCTACCT CCTGGGCTCA GACGATTCTT CCACCTAAGC
 CTCTTGAATA GTTGGGACTA TAGGCATGCA GCACCACAGC TGGCTAATTT TTTGTATTTA
 TTGTAAAGAT GGGATTCACC ATATTGTCCA GACTGGTCTT GAACACCTGA TCTCAAGTGA
 TCCACCCACC TGGGCCTCCC AAAGTGCTGT GATTATATGG
 N
 AGCACCTAGC TCCATCCTAG TTTCTGACTC AAACCAATAT TTGTGTATAC AGCTCATCCT
 CAGAATTGAT CTTCCATAGC CTAAACAGAG GTATGAGACA CAAGGAAAAT AGAGGTTACC
 CAGAAGAATG TTTAGAGCAT CCTGCCATTC ATCTTGAGAA GATTCACTGT CTACAACCAG
 AATTGAGTTG ACTTTGTCTT CCTCAGATGT GATTTTGATG TTCTTGTGAG GCGGGTTGGA
 GTCAGAAGGG CCATGGCTAT TTGAATAAGT GATGGCACAT TCCTCCAGTG AGTCCTCAGG
 GACTTCCTTT TCTTCAGCCT TCTGCTCCTC CCTGATGAGC CAGGTGGGAT AGAAATGACA
 GAAGATTAAA CAGAGAGGGA TTGGATCCCA GGGAGACCTA

  Submitted Frequency for ss50017592 back to top
There is no frequency submission for ss50017592.


  dbSNP summary of Genotypes for ss50017592 back to top
No sufficient data to compute Hardy-weinberg probability for ss50017592.


  Submitted individual genotype for ss50017592 back to top
There is no individual genotype data for ss50017592.

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