Submitter | Handle | ILLUMINA | Submitter SNP ID | HumanOmni2.5-4v1_B_rs6687776-128_T_R_1773065224 | RefSNP(rs#) | rs6687776 | Submitted Batch ID | HumanOmni2.5-4v1_B | Submitted Date | Jan 30, 2012 | Publication Cited | N.D. | First entry to dbSNP | Jan 30 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 | C/T | 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|ss481317791|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic GTATCAGCTC CACTTTGATT AATTG
Y
TTTGGCAATT CCAGGTCACA TGTGT
There is no frequency submission for ss481317791.
No sufficient data to compute Hardy-weinberg probability for ss481317791.
There is no individual genotype data for ss481317791.
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