| Submitter | | Handle | PJP | | Submitter SNP ID | SNP_152679_chr1_159460307 | | RefSNP(rs#) | rs5082 | | Submitted Batch ID | NSMB2011_SNP | | 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 | G/A | | Ancestral Allele | N.D. | | Allele Origin | N/A | | SNP Class | SNV | | CpG Code | N.D. |
| | Validation | | Validation Status | Not Validated | | HWE Goodness of Fit | not applicable | | Homozygote Detected | | | PCR Confirmed | | | In Expressed Sequence | |
| | Variation | | Frequency Submission | N.D. | | Genotype Summary | N.D. | | Genotype Submission | N.D. | | Haplotype | N.D. |
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>gnl|dbSNP|ss290646321|allelePos=52|len=103|taxid=9606|alleles='G/A'|mol=Genomic TCAGGTATAT TTGAGGTTCA TTCTTTTGAG ATCTGAGGTC CTTGGACTTG A
R
TGCAACAGGA AGCAGGATTC CAAGTTATTT CTCTGGAAAG CTCTGACATA T
There is no frequency submission for ss290646321.
No sufficient data to compute Hardy-weinberg probability for ss290646321.
There is no individual genotype data for ss290646321.
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