Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanHap300v1.1_rs1002244 | RefSNP(rs#) | rs1002244 | Submitted Batch ID | HumanHap300v1.1 | Submitted Date | Nov 09, 2006 | Publication Cited | N.D. | First entry to dbSNP | Nov 9 2006 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 | INFINIUM-II | Ascertainment Samplesize | 270 | Population | N.D. |
| Allele | Observed Allele | A/G | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | SNV | 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|ss66539192|allelePos=51|len=101|taxid=9606|alleles='A/G'|mol=Genomic TTGTTGTGGA TTTGCAGATA GATTTGTGCC ACAAAATGTC ATAATTTTAT
R
CACACTAATG TAACAAAGAG AAATCTTAAC GAGATCGAGT GTTTTTCATG
There is no frequency submission for ss66539192.
No sufficient data to compute Hardy-weinberg probability for ss66539192.
There is no individual genotype data for ss66539192.
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