Submitter | Handle | PJP | Submitter SNP ID | DIP_123474_chr11_2939323 | RefSNP(rs#) | rs34999812 | Submitted Batch ID | NSMB2011_INDEL | Submitted Date | Jan 21, 2011 | Publication Cited | [1] Impact of chromatin structure on sequence variability in the human genome | First entry to dbSNP | Jan 21 2011 12:00:00:000AM |
| Resource Links | Submitted Gene Name | N.D | Submitted Gene ID | N.D. | Submitted SNP Synonyms | N.D | Submitted linkout | N.D |
| Assay | Species | Homo sapiens | Molecular Type | Genomic | Method | TRACESALIGNMENT | Ascertainment Samplesize | N.D. | Population | N.D. |
| Allele | Observed Allele | -/A | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | DIV | CpG Code | N.D. |
| | Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>gnl|dbSNP|ss294685770|allelePos=52|len=103|taxid=9606|alleles='-/A'|mol=Genomic AAAATGCCTA TTTCTCTCCC AACCCTCCAC GGCTTAAAAA AAAAAAAAAA A
N
CCAACATAAA GAGGGAAGAC AAGTAGCCAA CCAATGGAGA GACTGCTATG A
There is no frequency submission for ss294685770.
No sufficient data to compute Hardy-weinberg probability for ss294685770.
There is no individual genotype data for ss294685770.
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