| Submitter | | Handle | PJP | | Submitter SNP ID | DIP_269535_chr14_50482026 | | RefSNP(rs#) | rs71121614 | | 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 | -/T | | 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|ss294831831|allelePos=52|len=103|taxid=9606|alleles='-/T'|mol=Genomic TTTCCTTTTT CTTTTCTTTT TCTTTCTTCT TCTTCTTTTT TTTTTTTTTT T
N
GAGACGGAGT CTCACTCTGT TGCCCAGGCT GGAGTGCAGT GGCGCGATCT C
There is no frequency submission for ss294831831.
No sufficient data to compute Hardy-weinberg probability for ss294831831.
There is no individual genotype data for ss294831831.
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