| Submitter | | Handle | PJP | | Submitter SNP ID | SNP_3091321_chr6_2898444 | | RefSNP(rs#) | rs3818276 | | 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 | A/G | | 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|ss293584963|allelePos=52|len=103|taxid=9606|alleles='A/G'|mol=Genomic CCGGAGAGAG CAACTCCGCA ATTTTACCTG AGCGGAAGAA TTCAAGACCG C
R
TTAGATAGGG GCGGCTGCGG ATCCCCGACA CATCAGGAAT CGGCTGGGGC C
There is no frequency submission for ss293584963.
No sufficient data to compute Hardy-weinberg probability for ss293584963.
There is no individual genotype data for ss293584963.
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