Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanOmni5-4v1_B_kgp11943769-0_T_R_1797691884 | RefSNP(rs#) | rs6256 | Submitted Batch ID | HumanOmni5-4v1_B | Submitted Date | Jun 22, 2012 | Publication Cited | N.D. | First entry to dbSNP | Jun 22 2012 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 | ILLUMINA-CHIP | Ascertainment Samplesize | 2 | Population | N.D. |
| Allele | Observed Allele | G/T | Ancestral Allele | N.D. | Allele Origin | T:Germline C:Germline | SNP Class | SNV | CpG Code | N.D. |
| | Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
|
>gnl|dbSNP|ss533352697|allelePos=26|len=51|taxid=9606|alleles='G/T'|mol=Genomic ACCAAGACAT TGTCTTCCTT TTTTC
K
GGGCCTCTGG GAACCAGCAT CTCTG
There is no frequency submission for ss533352697.
No sufficient data to compute Hardy-weinberg probability for ss533352697.
There is no individual genotype data for ss533352697.
|