| Submitter | | Handle | PJP | | Submitter SNP ID | SNP_3091320_chr6_2898251 | | RefSNP(rs#) | rs2244693 | | 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 | T/C | | 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. |
|
>gnl|dbSNP|ss293584962|allelePos=52|len=103|taxid=9606|alleles='T/C'|mol=Genomic CTGCAGACGC GGGAGGCCCC GAGCCGGAGA CGCTCGTGTG AACACAGGCG C
Y
GCTCCTGTCA CGGCCCCTTA CTCGCCTTGC TGACTTTAAA CAGTCTCTCC T
There is no frequency submission for ss293584962.
No sufficient data to compute Hardy-weinberg probability for ss293584962.
There is no individual genotype data for ss293584962.
| 
