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Submitted SNP(ss) Details: ss3181517           
Submitter
HandleGENAISSANCE
Submitter SNP IDGEN3200
RefSNP(rs#)rs2227264
Submitted Batch ID010601
Submitted DateJul 19, 2001
Publication Cited[1] Haplotype Variation and Linkage Disequilibrium in 313 Human Genes
First entry to dbSNPJul 19 2001 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodSequencing
Ascertainment Samplesize1968
PopulationGENAISSANCE_POP
Allele
Observed AlleleT/G
Ancestral Allele
Allele OriginN/A
SNP ClassSNV
CpG CodenonCpG
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.
Comment
Variation [T/G (G) Ile 26 Ser] mapped to exon 1 at nucleotide position 43855 in AC004979.1.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss3181517|allelePos=101|len=201|taxid=9606|alleles='T/G'|mol=Genomic
 AGTGAGAGCC TCCTCTCCCC AGCCATGCTG AGCGCTGGCC TAGGACTGCT GATGCTGGTG
 GCAGTGGTTG AATTTCTCAT CGGTTTAATT GGAAATGGAA
 K
 CCTGGTGGTC TGGAGTTTTA GAGAATGGAT CAGAAAATTC AACTGGTCCT CATATAACCT
 CATTATCCTG GGCCTGGCTG GCTGCCGATT TCTCCTGCAG

  Submitted Frequency for ss3181517 back to top
There is no frequency submission for ss3181517.


  dbSNP summary of Genotypes for ss3181517 back to top
No sufficient data to compute Hardy-weinberg probability for ss3181517.


  Submitted individual genotype for ss3181517 back to top
There is no individual genotype data for ss3181517.

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